Prescription drug · ANDA
Valsartan NDC 70771-1885
Valsartan 320 mg/1 · Tablet, Film coated · Oral · Zydus Lifesciences Limited
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 70771-1885-9 | 70771188509 | 90 TABLET, FILM COATED in 1 BOTTLE (70771-1885-9)Marketed from Aug 30, 2024 |
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)
- Valsartan
- Generic name (nonproprietary)
- valsartan
- Active ingredients
- Valsartan — 320 mg/1
- Dosage form
- Tablet, Film coated
- Route
- Oral
- Labeler
- Zydus Lifesciences Limited
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 218991
- Marketing start
- Listing expires
- Other FDA classes
- Angiotensin 2 Receptor Antagonists (Mechanism)
- Identifiers
- Product ID 70771-1885_a69225f3-d9ea-4ed4-b7ab-225147cad486SPL ID a69225f3-d9ea-4ed4-b7ab-225147cad486SPL set ID 1b60c816-7399-42c3-8b74-4dc9d82873ecRxCUI 349199, 349200, 349201, 349483UNII 80M03YXJ7IUPC 0372578134167
- Pharmacologic class
- Angiotensin 2 Receptor Blocker
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
N470771188509followed by a unit qualifier and the quantityPackage 70771-1885-09. 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 .
Other NDCs under ANDA 218991
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 |
|---|---|---|---|---|
| Valsartan | Valsartan 40 mg/1 | Tablet, Film coatedOral | PD-Rx Pharmaceuticals, Inc. | 72789-553 |
| Valsartan | Valsartan 160 mg/1 | Tablet, Film coatedOral | Viona Pharmaceuticals Inc | 72578-133 |
| Valsartan | Valsartan 40 mg/1 | Tablet, Film coatedOral | Viona Pharmaceuticals Inc | 72578-131 |
| Valsartan | Valsartan 80 mg/1 | Tablet, Film coatedOral | Viona Pharmaceuticals Inc | 72578-132 |
| Valsartan | Valsartan 320 mg/1 | Tablet, Film coatedOral | Viona Pharmaceuticals Inc | 72578-134 |
| Valsartan | Valsartan 80 mg/1 | Tablet, Film coatedOral | Zydus Lifesciences Limited | 70771-1883 |
| Valsartan | Valsartan 40 mg/1 | Tablet, Film coatedOral | Zydus Lifesciences Limited | 70771-1882 |
| Valsartan | Valsartan 160 mg/1 | Tablet, Film coatedOral | Zydus Lifesciences Limited | 70771-1884 |