NDC product
Amoxicillin and Clavulanate Potassium
NDC 0781-6102 · Sandoz Inc
Key facts
| Product NDC | 0781-6102 |
|---|---|
| Proprietary name | Amoxicillin and Clavulanate Potassium |
| Nonproprietary name | Amoxicillin and Clavulanate Potassium |
| Substances | AMOXICILLIN, CLAVULANATE POTASSIUM |
| Dosage form | POWDER, FOR SUSPENSION |
| Route | ORAL |
| Labeler | Sandoz Inc |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA065066 |
| Pharmacologic classes | Penicillin-class Antibacterial [EPC], Penicillins [CS], beta Lactamase Inhibitor [EPC], beta Lactamase Inhibitors [MoA] |
| Marketing start | Jun 5, 2002 |
| Listing certified through | Dec 31, 2026 |
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: