Prescription drug · ANDA
Eletriptan hydrobromide NDC 70771-1108
Eletriptan hydrobromide 40 mg/1 · Tablet, Film coated · Oral · Zydus Lifesciences Limited
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 70771-1108-3 | 70771110803 | 30 TABLET, FILM COATED in 1 BOTTLE (70771-1108-3)Marketed from Jul 12, 2017 | |
| 70771-1108-4 | 70771110804 | 10 BLISTER PACK in 1 CARTON (70771-1108-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70771-1108-2)Marketed from Jul 12, 2017 | |
| 70771-1108-5 | 70771110805 | 500 TABLET, FILM COATED in 1 BOTTLE (70771-1108-5)Marketed from Jul 12, 2017 | |
| 70771-1108-6 | 70771110806 | 1 BLISTER PACK in 1 CARTON (70771-1108-6) / 6 TABLET, FILM COATED in 1 BLISTER PACKMarketed from Jul 12, 2017 |
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)
- Eletriptan hydrobromide
- Generic name (nonproprietary)
- eletriptan hydrobromide
- Active ingredients
- Eletriptan hydrobromide — 40 mg/1
- Dosage form
- Tablet, Film coated
- Route
- Oral
- Labeler
- Zydus Lifesciences LimitedNDC labeler code 70771
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 206409
- Marketing start
- Listing expires
- Other FDA classes
- Serotonin 1b Receptor Agonists (Mechanism)Serotonin 1d Receptor Agonists (Mechanism)
- Identifiers
- Product ID 70771-1108_b0459347-b3de-466e-b386-85665dd294c9SPL ID b0459347-b3de-466e-b386-85665dd294c9SPL set ID 481ae7d4-9e57-424a-9d07-2920954b6ddcRxCUI 359493, 359494UNII M41W832TA3
- Pharmacologic class
- Serotonin-1b and Serotonin-1d Receptor 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
N470771110803followed by a unit qualifier and the quantityPackage 70771-1108-03. 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 .
About NDC 70771-1108
- What is NDC 70771-1108?
- 70771-1108 is the product NDC for Eletriptan hydrobromide, Eletriptan hydrobromide 40 mg/1 tablet, film coated, listed with the FDA by Zydus Lifesciences Limited. It has 4 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Eletriptan hydrobromide.
- What is the active ingredient?
- Eletriptan hydrobromide.
- Who is the labeler?
- Zydus Lifesciences Limited, NDC labeler code 70771. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Eletriptan hydrobromide?
- 16 other product NDCs are listed under this name. See all Eletriptan hydrobromide NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Eletriptan hydrobromide products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Eletriptan Hydrobromide | Eletriptan hydrobromide 20 mg/1 | Tablet, Film coatedOral | Apnar Pharma LP | 24689-167 | 24689-0167-01 |
| Eletriptan Hydrobromide | Eletriptan hydrobromide 40 mg/1 | Tablet, Film coatedOral | Apnar Pharma LP | 24689-168 | 24689-0168-01 |
| Eletriptan hydrobromide | Eletriptan hydrobromide 20 mg/1 | Tablet, Film coatedOral | Camber Pharmaceuticals, Inc. | 31722-443 | 31722-0443-31 |
| Eletriptan hydrobromide | Eletriptan hydrobromide 40 mg/1 | Tablet, Film coatedOral | Camber Pharmaceuticals, Inc. | 31722-444 | 31722-0444-3131722-0444-33 |
| Eletriptan Hydrobromide | Eletriptan hydrobromide 40 mg/1 | Tablet, Film coatedOral | Advanced Rx of Tennessee, LLC | 80425-0408 | 80425-0408-01 |
| Eletriptan Hydrobromide | Eletriptan hydrobromide 20 mg/1 | Tablet, Film coatedOral | Aurobindo Pharma Limited | 59651-104 | 59651-0104-69 |
| Eletriptan Hydrobromide | Eletriptan hydrobromide 40 mg/1 | Tablet, Film coatedOral | Aurobindo Pharma Limited | 59651-105 | 59651-0105-6959651-0105-93 |
| Eletriptan Hydrobromide | Eletriptan hydrobromide 40 mg/1 | Tablet, Film coatedOral | Bryant Ranch Prepack | 63629-8320 | 63629-8320-0163629-8320-02 |
| Eletriptan Hydrobromide | Eletriptan hydrobromide 20 mg/1 | Tablet, Film coatedOral | Mylan Pharmaceuticals Inc. | 0378-4287 | 00378-4287-85 |
| Eletriptan Hydrobromide | Eletriptan hydrobromide 40 mg/1 | Tablet, Film coatedOral | Mylan Pharmaceuticals Inc. | 0378-4288 | 00378-4288-0800378-4288-85 |
Other NDCs under ANDA 206409
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 |
|---|---|---|---|---|
| Eletriptan hydrobromide | Eletriptan hydrobromide 20 mg/1 | Tablet, Film coatedOral | Zydus Pharmaceuticals USA Inc. | 68382-922 |
| Eletriptan hydrobromide | Eletriptan hydrobromide 40 mg/1 | Tablet, Film coatedOral | Zydus Pharmaceuticals USA Inc. | 68382-923 |
| Eletriptan hydrobromide | Eletriptan hydrobromide 20 mg/1 | Tablet, Film coatedOral | Zydus Lifesciences Limited | 70771-1107 |
| Eletriptan hydrobromide | Eletriptan hydrobromide 40 mg/1 | Tablet, Film coatedOral | Bryant Ranch Prepack | 71335-2983 |