Prescription drug · ANDA
Hydrocodone Bitartrate and Acetaminophen NDC 63629-5422
Hydrocodone bitartrate 5 mg/1; Acetaminophen 325 mg/1 · Tablet · Oral · Bryant Ranch Prepack
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 63629-5422-0 | 6362954220063629542200 | 10 TABLET in 1 BOTTLE (63629-5422-0)Marketed from Jul 25, 2017 | |
| 63629-5422-1 | 6362954220163629542201 | 30 TABLET in 1 BOTTLE (63629-5422-1)Marketed from Oct 6, 2014 | |
| 63629-5422-2 | 6362954220263629542202 | 120 TABLET in 1 BOTTLE (63629-5422-2)Marketed from Oct 14, 2014 | |
| 63629-5422-3 | 6362954220363629542203 | 20 TABLET in 1 BOTTLE (63629-5422-3)Marketed from Oct 6, 2014 | |
| 63629-5422-4 | 6362954220463629542204 | 60 TABLET in 1 BOTTLE (63629-5422-4)Marketed from Oct 6, 2014 | |
| 63629-5422-5 | 6362954220563629542205 | 90 TABLET in 1 BOTTLE (63629-5422-5)Marketed from Oct 6, 2014 | |
| 63629-5422-6 | 6362954220663629542206 | 50 TABLET in 1 BOTTLE (63629-5422-6)Marketed from Dec 22, 2019 | |
| 63629-5422-7 | 6362954220763629542207 | 40 TABLET in 1 BOTTLE (63629-5422-7)Marketed from Oct 23, 2014 | |
| 63629-5422-8 | 6362954220863629542208 | 15 TABLET in 1 BOTTLE (63629-5422-8)Marketed from Nov 3, 2014 | |
| 63629-5422-9 | 6362954220963629542209 | 84 TABLET in 1 BOTTLE (63629-5422-9)Marketed from Dec 1, 2014 |
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)
- Hydrocodone Bitartrate and Acetaminophen
- Generic name (nonproprietary)
- hydrocodone bitartrate and acetaminophen
- Active ingredients
- Hydrocodone bitartrate — 5 mg/1Acetaminophen — 325 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- Bryant Ranch PrepackNDC labeler code 63629
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 040736
- Marketing start
- Listing expires
- DEA schedule
- CII
- Other FDA classes
- Opioid Agonists (Mechanism)
- Identifiers
- Product ID 63629-5422_1960bda9-b48f-4f7a-949a-b9fb8ab1ed67SPL ID 1960bda9-b48f-4f7a-949a-b9fb8ab1ed67SPL set ID a200d099-fa55-4ef1-b8d7-936a7da1db00RxCUI 857002UNII NO70W886KK, 362O9ITL9D
- Pharmacologic class
- Opioid Agonist
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
N463629542200followed by a unit qualifier and the quantityPackage 63629-5422-00. 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 . This label includes a boxed warning.
Indications (excerpt from the label)
INDICATIONS AND USAGE Hydrocodone Bitartrate and Acetaminophen Tablets are indicated for the management of pain severe enough to require an opioid analgesic and for which alternative treatments are inadequate. Limitations of Use Because of the risks of addiction, abuse, and misuse, with opioids, even at recommended doses [see WARNINGS ], reserve Hydrocodone Bitartrate and Acetaminophen Tablets for use in patients for whom alternative treatment options (e.g., non-opioid analgesics): have not been tolerated, or are not expected to be tolerated, have not provided adequate analgesia, or are not expected to provide adequate analgesia
Excerpt only. Read the full label for complete information.
About NDC 63629-5422
- What is NDC 63629-5422?
- 63629-5422 is the product NDC for Hydrocodone Bitartrate and Acetaminophen, Hydrocodone bitartrate 5 mg/1; Acetaminophen 325 mg/1 tablet, 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?
- Hydrocodone Bitartrate and Acetaminophen.
- What is the active ingredient?
- Hydrocodone bitartrate, Acetaminophen.
- Who is the labeler?
- Bryant Ranch Prepack, NDC labeler code 63629. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Hydrocodone Bitartrate and Acetaminophen?
- 202 other product NDCs are listed under this name. See all Hydrocodone Bitartrate and Acetaminophen NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Hydrocodone Bitartrate and Acetaminophen products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Hydrocodone Bitartrate and Acetaminophen | Hydrocodone bitartrate 5 mg/1; Acetaminophen 325 mg/1 | TabletOral | St. Mary's Medical Park Pharmacy | 60760-873 | 60760-0873-3060760-0873-60 |
| Hydrocodone Bitartrate and Acetaminophen | Acetaminophen 325 mg/1; Hydrocodone bitartrate 10 mg/1 | TabletOral | St. Mary's Medical Park Pharmacy | 60760-872 | 60760-0872-3060760-0872-60 |
| hydrocodone bitartrate and acetaminophen | Hydrocodone bitartrate 5 mg/1; Acetaminophen 325 mg/1 | TabletOral | Strides Pharma Science Limited | 64380-440 | 64380-0440-01 |
| hydrocodone bitartrate and acetaminophen | Hydrocodone bitartrate 7.5 mg/1; Acetaminophen 325 mg/1 | TabletOral | Strides Pharma Science Limited | 64380-441 | 64380-0441-01 |
| hydrocodone bitartrate and acetaminophen | Hydrocodone bitartrate 10 mg/1; Acetaminophen 325 mg/1 | TabletOral | Strides Pharma Science Limited | 64380-442 | 64380-0442-01 |
| hydrocodone bitartrate and acetaminophen | Hydrocodone bitartrate 5 mg/1; Acetaminophen 325 mg/1 | TabletOral | Proficient Rx LP | 82804-306 | 82804-0306-12 |
| Hydrocodone Bitartrate and Acetaminophen | Hydrocodone bitartrate 2.5 mg/1; Acetaminophen 325 mg/1 | TabletOral | Camber Pharmaceuticals, Inc. | 31722-940 | 31722-0940-01 |
| Hydrocodone Bitartrate and Acetaminophen | Hydrocodone bitartrate 7.5 mg/1; Acetaminophen 325 mg/1 | TabletOral | Camber Pharmaceuticals, Inc. | 31722-942 | 31722-0942-0131722-0942-05 |
| Hydrocodone Bitartrate And Acetaminophen | Hydrocodone bitartrate 5 mg/1; Acetaminophen 325 mg/1 | TabletOral | St. Mary's Medical Park Pharmacy | 60760-870 | 60760-0870-3060760-0870-60 |
| Hydrocodone Bitartrate And Acetaminophen | Hydrocodone bitartrate 10 mg/15mL; Acetaminophen 300 mg/15mL | LiquidOral | Hikma Pharmaceuticals USA Inc. | 0054-0843 | 00054-0843-63 |
Other NDCs under ANDA 040736
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 |
|---|---|---|---|---|
| Hydrocodone Bitartrate and Acetaminophen | Hydrocodone bitartrate 5 mg/1; Acetaminophen 325 mg/1 | TabletOral | AvPAK | 50268-401 |
| Hydrocodone Bitartrate and Acetaminophen | Hydrocodone bitartrate 10 mg/1; Acetaminophen 325 mg/1 | TabletOral | AvPAK | 50268-402 |
| Hydrocodone Bitartrate and Acetaminophen | Hydrocodone bitartrate 5 mg/1; Acetaminophen 325 mg/1 | TabletOral | Amneal Pharmaceuticals of New York LLC | 53746-109 |
| Hydrocodone Bitartrate and Acetaminophen | Hydrocodone bitartrate 5 mg/1; Acetaminophen 325 mg/1 | TabletOral | Proficient Rx LP | 63187-112 |