NDC product
Allopurinol
NDC 16571-885 · Rising Pharma Holdings, Inc.
Key facts
| Product NDC | 16571-885 |
|---|---|
| Proprietary name | Allopurinol |
| Nonproprietary name | allopurinol |
| Substances | ALLOPURINOL |
| Dosage form | TABLET |
| Route | ORAL |
| Labeler | Rising Pharma Holdings, Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA AUTHORIZED GENERIC |
| Application number | NDA016084 |
| Pharmacologic classes | Xanthine Oxidase Inhibitor [EPC], Xanthine Oxidase Inhibitors [MoA] |
| Marketing start | Sep 21, 2023 |
| Listing certified through | Dec 31, 2027 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date: