NDC product
Amantadine Hydrochloride
NDC 60760-779 · ST. MARY'S MEDICAL PARK PHARMACY
Key facts
| Product NDC | 60760-779 |
|---|---|
| Proprietary name | Amantadine Hydrochloride |
| Nonproprietary name | Amantadine Hydrochloride |
| Substances | AMANTADINE HYDROCHLORIDE |
| Dosage form | CAPSULE |
| Route | ORAL |
| Labeler | ST. MARY'S MEDICAL PARK PHARMACY |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA212044 |
| Pharmacologic classes | Influenza A M2 Protein Inhibitor [EPC], M2 Protein Inhibitors [MoA] |
| Marketing start | May 21, 2020 |
| Listing certified through | Dec 31, 2026 |
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: