Prescription drug · ANDA
Valacyclovir Hydrochloride NDC 71335-0708
Valacyclovir hydrochloride 500 mg/1 · Tablet, Film coated · Oral · Bryant Ranch Prepack
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 71335-0708-0 | 71335070800 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-0708-0)Marketed from Feb 10, 2022 | |
| 71335-0708-1 | 71335070801 | 15 TABLET, FILM COATED in 1 BOTTLE (71335-0708-1)Marketed from Jan 11, 2022 | |
| 71335-0708-2 | 71335070802 | 10 TABLET, FILM COATED in 1 BOTTLE (71335-0708-2)Marketed from Apr 12, 2018 | |
| 71335-0708-3 | 71335070803 | 4 TABLET, FILM COATED in 1 BOTTLE (71335-0708-3)Marketed from Apr 20, 2022 | |
| 71335-0708-4 | 71335070804 | 7 TABLET, FILM COATED in 1 BOTTLE (71335-0708-4)Marketed from Apr 24, 2018 | |
| 71335-0708-5 | 71335070805 | 20 TABLET, FILM COATED in 1 BOTTLE (71335-0708-5)Marketed from Oct 19, 2021 | |
| 71335-0708-6 | 71335070806 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-0708-6)Marketed from Feb 26, 2018 | |
| 71335-0708-7 | 71335070807 | 8 TABLET, FILM COATED in 1 BOTTLE (71335-0708-7)Marketed from Aug 16, 2018 | |
| 71335-0708-8 | 71335070808 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-0708-8)Marketed from Jun 14, 2019 | |
| 71335-0708-9 | 71335070809 | 14 TABLET, FILM COATED in 1 BOTTLE (71335-0708-9)Marketed from Apr 22, 2019 |
How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- Valacyclovir Hydrochloride
- Generic name (nonproprietary)
- valacyclovir hydrochloride
- Active ingredients
- Valacyclovir hydrochloride — 500 mg/1
- Dosage form
- Tablet, Film coated
- Route
- Oral
- Labeler
- Bryant Ranch PrepackNDC labeler code 71335
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 090682
- Marketing start
- Listing expires
- Other FDA classes
- DNA Polymerase Inhibitors (Mechanism)Nucleoside Analog (EXT)
- Identifiers
- Product ID 71335-0708_58ea1068-9302-4edd-acfa-4f539aa58427SPL ID 58ea1068-9302-4edd-acfa-4f539aa58427SPL set ID 93dccd99-d28b-4c47-872c-c3c0001b8a7fRxCUI 313565UNII G447S0T1VC
- Pharmacologic class
- Herpes Simplex Virus Nucleoside Analog DNA Polymerase Inhibitor; Herpes Zoster Virus Nucleoside Analog DNA Polymerase Inhibitor; Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N471335070800followed by a unit qualifier and the quantityPackage 71335-0708-00. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective .
Indications (excerpt from the label)
Valacyclovir hydrochloride is a deoxynucleoside analogue DNA polymerase inhibitor indicated for: Adult Patients (1.1) Cold Sores (Herpes Labialis) Genital Herpes Treatment in immunocompetent patients (initial or recurrent episode) Suppression in immunocompetent or HIV-1-infected patients Reduction of transmission Herpes Zoster Pediatric Patients (1.2) Cold Sores (Herpes Labialis) Chickenpox Limitations of Use (1.3) The efficacy and safety of valacyclovir tablets have not been established in immunocompromised patients other than for the suppression of genital herpes in HIV-1-infected patients. 1.1 Adult Patients Cold Sores (Herpes Labialis) Valacyclovir tablets are indicated for treatment of …
Excerpt only. Read the full label for complete information.
About NDC 71335-0708
- What is NDC 71335-0708?
- 71335-0708 is the product NDC for Valacyclovir Hydrochloride, Valacyclovir hydrochloride 500 mg/1 tablet, film coated, listed with the FDA by Bryant Ranch Prepack. It has 10 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Valacyclovir Hydrochloride.
- What is the active ingredient?
- Valacyclovir hydrochloride.
- Who is the labeler?
- Bryant Ranch Prepack, NDC labeler code 71335. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Valacyclovir Hydrochloride?
- 56 other product NDCs are listed under this name. See all Valacyclovir Hydrochloride NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Valacyclovir Hydrochloride products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Valacyclovir Hydrochloridevalacyclovir | Valacyclovir hydrochloride 1 g/1 | Tablet, Film coatedOral | Northwind Health Company, LLC | 82868-106 | 82868-0106-21 |
| Valacyclovir Hydrochloridevalacyclovir | Valacyclovir hydrochloride 500 mg/1 | Tablet, Film coatedOral | Safecor Health LLC | 48433-144 | 48433-0144-03 |
| Valacyclovir Hydrochloride | Valacyclovir hydrochloride 500 mg/1 | Tablet, Film coatedOral | Preferred Pharmaceuticals Inc. | 68788-8904 | 68788-8904-0368788-8904-09 |
| Valacyclovir Hydrochloride | Valacyclovir hydrochloride 1 g/1 | Tablet, Film coatedOral | Preferred Pharmaceuticals Inc. | 68788-8820 | 68788-8820-0068788-8820-0168788-8820-02+4 more |
| Valacyclovir Hydrochloride | Valacyclovir hydrochloride 1 g/1 | Tablet, Film coatedOral | St. Mary's Medical Park Pharmacy | 60760-757 | 60760-0757-42 |
| Valacyclovir Hydrochloridevalacyclovir | Valacyclovir hydrochloride 500 mg/1 | Tablet, Film coatedOral | Northwind Health Company, LLC | 82868-055 | 82868-0055-21 |
| Valacyclovir Hydrochloridevalacyclovir | Valacyclovir hydrochloride 500 mg/1 | Tablet, Film coatedOral | Preferred Pharmaceuticals Inc. | 68788-8482 | 68788-8482-0368788-8482-09 |
| Valacyclovir Hydrochloride | Valacyclovir hydrochloride 1 g/1 | Tablet, Film coatedOral | Northwind Health Company, LLC | 51655-703 | 51655-0703-0451655-0703-2151655-0703-53 |
| Valacyclovir Hydrochloride | Valacyclovir hydrochloride 500 mg/1 | Tablet, Film coatedOral | Northwind Health Company, LLC | 51655-633 | 51655-0633-2151655-0633-84 |
| Valacyclovir Hydrochloride | Valacyclovir hydrochloride 1 g/1 | Tablet, Film coatedOral | REMEDYREPACK INC. | 70518-3359 | 70518-3359-0170518-3359-0270518-3359-03 |
Other NDCs under ANDA 090682
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Valacyclovir Hydrochloride | Valacyclovir hydrochloride 500 mg/1 | Tablet, Film coatedOral | Bryant Ranch Prepack | 72162-2366 |
| Valacyclovir Hydrochloride | Valacyclovir hydrochloride 1 g/1 | Tablet, Film coatedOral | NuCare Pharmacuticals,Inc. | 68071-1548 |
| Valacyclovir Hydrochloride | Valacyclovir hydrochloride 500 mg/1 | Tablet, Film coatedOral | PD-Rx Pharmaceuticals, Inc. | 43063-730 |
| Valacyclovir Hydrochloride | Valacyclovir hydrochloride 500 mg/1 | Tablet, Film coatedOral | NuCare Pharmaceuticals,Inc. | 68071-2738 |
| Valacyclovir Hydrochloride | Valacyclovir hydrochloride 1 g/1 | Tablet, Film coatedOral | Sportpharm LLC | 85766-026 |
| Valacyclovir Hydrochloride | Valacyclovir hydrochloride 500 mg/1 | Tablet, Film coatedOral | A-S Medication Solutions | 50090-5852 |
| Valacyclovir Hydrochloride | Valacyclovir hydrochloride 1 g/1 | Tablet, Film coatedOral | NorthStar Rx LLC | 16714-697 |
| Valacyclovir Hydrochloride | Valacyclovir hydrochloride 500 mg/1 | Tablet, Film coatedOral | NorthStar Rx LLC | 16714-698 |
| Valacyclovir Hydrochloride | Valacyclovir hydrochloride 500 mg/1 | Tablet, Film coatedOral | Cardinal Health 107, LLC | 55154-7985 |
| Valacyclovir Hydrochloride | Valacyclovir hydrochloride 500 mg/1 | Tablet, Film coatedOral | American Health Packaging | 68084-215 |
| Valacyclovir Hydrochloride | Valacyclovir hydrochloride 500 mg/1 | Tablet, Film coatedOral | PD-Rx Pharmaceuticals, Inc. | 72789-264 |
| Valacyclovir Hydrochloride | Valacyclovir hydrochloride 500 mg/1 | Tablet, Film coatedOral | PD-Rx Pharmaceuticals, Inc. | 72789-263 |
| Valacyclovir Hydrochloride | Valacyclovir hydrochloride 500 mg/1 | Tablet, Film coatedOral | Sportpharm LLC | 85766-054 |
| Valacyclovir Hydrochloride | Valacyclovir hydrochloride 1 g/1 | Tablet, Film coatedOral | American Health Packaging | 68084-309 |
| Valacyclovir Hydrochloride | Valacyclovir hydrochloride 500 mg/1 | Tablet, Film coatedOral | Asclemed USA, Inc. | 76420-053 |
| Valacyclovir Hydrochloride | Valacyclovir hydrochloride 1 g/1 | Tablet, Film coatedOral | Preferred Pharmaceuticals Inc. | 68788-8820 |
| Valacyclovir Hydrochloride | Valacyclovir hydrochloride 500 mg/1 | Tablet, Film coatedOral | REMEDYREPACK INC. | 70518-2266 |
| Valacyclovir Hydrochloride | Valacyclovir hydrochloride 1 g/1 | Tablet, Film coatedOral | St. Mary's Medical Park Pharmacy | 60760-757 |
| Valacyclovir Hydrochloride | Valacyclovir hydrochloride 1 g/1 | Tablet, Film coatedOral | Bryant Ranch Prepack | 71335-1862 |
| Valacyclovir Hydrochloride | Valacyclovir hydrochloride 1 g/1 | Tablet, Film coatedOral | NuCare Pharmaceuticals,Inc. | 68071-4728 |
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