Prescription drug · ANDA
Allopurinol NDC 70771-1907
Allopurinol 200 mg/1 · Tablet · Oral · Zydus Lifesciences Limited
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 70771-1907-0 | 70771190700 | 1000 TABLET in 1 BOTTLE (70771-1907-0)Marketed from Jun 17, 2025 | |
| 70771-1907-9 | 70771190709 | 90 TABLET in 1 BOTTLE (70771-1907-9)Marketed from Jun 17, 2025 |
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)
- Allopurinol
- Generic name (nonproprietary)
- allopurinol
- Active ingredients
- Allopurinol — 200 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- Zydus Lifesciences Limited
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 210117
- Marketing start
- Listing expires
- Other FDA classes
- Xanthine Oxidase Inhibitors (Mechanism)
- Identifiers
- Product ID 70771-1907_183fab96-5c7b-4fcc-a475-5d1832bbf9c6SPL ID 183fab96-5c7b-4fcc-a475-5d1832bbf9c6SPL set ID 9232f484-a5f6-4c63-b7f4-b510d2827159RxCUI 197319, 197320, 245422UNII 63CZ7GJN5I
- Pharmacologic class
- Xanthine Oxidase 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
N470771190700followed by a unit qualifier and the quantityPackage 70771-1907-00. 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
Label details couldn’t be retrieved right now. Open the label on DailyMed.
Other NDCs under ANDA 210117
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 |
|---|---|---|---|---|
| Allopurinol | Allopurinol 200 mg/1 | TabletOral | Zydus Pharmaceuticals (USA) Inc. | 70710-2009 |
| Allopurinol | Allopurinol 100 mg/1 | TabletOral | Zydus Pharmaceuticals (USA) Inc. | 70710-1209 |
| Allopurinol | Allopurinol 300 mg/1 | TabletOral | Zydus Pharmaceuticals (USA) Inc. | 70710-1210 |
| Allopurinol | Allopurinol 300 mg/1 | TabletOral | Zydus Lifesciences Limited | 70771-1127 |
| Allopurinol | Allopurinol 100 mg/1 | TabletOral | Zydus Lifesciences Limited | 70771-1126 |
| Allopurinol | Allopurinol 100 mg/1 | TabletOral | Major Pharmaceuticals | 0904-7041 |
| Allopurinol | Allopurinol 100 mg/1 | TabletOral | Cardinal Health 107, LLC | 55154-2338 |