NDC product
Amoxicillin and Clavulanate Potassium
NDC 68788-4179 · Preferred Pharmaceuticals Inc.
Key facts
| Product NDC | 68788-4179 |
|---|---|
| Proprietary name | Amoxicillin and Clavulanate Potassium |
| Nonproprietary name | Amoxicillin and Clavulanate Potassium |
| Substances | AMOXICILLIN, CLAVULANIC ACID |
| Dosage form | POWDER, FOR SUSPENSION |
| Route | ORAL |
| Labeler | Preferred Pharmaceuticals Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA065191 |
| Pharmacologic classes | Penicillin-class Antibacterial [EPC], Penicillins [CS], beta Lactamase Inhibitor [EPC], beta Lactamase Inhibitors [MoA] |
| Marketing start | Jul 31, 2026 |
| 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: