NDC product
Diclofenac Sodium and Misoprostol
NDC 65162-436 · Amneal Pharmaceuticals LLC
Key facts
| Product NDC | 65162-436 |
|---|---|
| Proprietary name | Diclofenac Sodium and Misoprostol |
| Nonproprietary name | Diclofenac Sodium and Misoprostol |
| Substances | DICLOFENAC SODIUM, MISOPROSTOL |
| Dosage form | TABLET, DELAYED RELEASE |
| Route | ORAL |
| Labeler | Amneal Pharmaceuticals LLC |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA203995 |
| Pharmacologic classes | Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Decreased Prostaglandin Production [PE], Nonsteroidal Anti-inflammatory Drug [EPC], Prostaglandin E1 Analog [EPC] and 2 more |
| Marketing start | Dec 1, 2016 |
| Listing certified through | Dec 31, 2027 |
At a glance
- 1–9 Package NDCs
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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: