Amoxicillin and Clavulanate Potassium
- Product NDC
- 68071-1865
- 11-digit product format
- 680711865
- Labeler code
- 68071
- Product ID
- 68071-1865_bb26d8a2-c227-3dd5-e053-2995a90a2bce
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin and Clavulanate Potassium
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA065191
- Marketing category
- ANDA
- Marketing start
- 2007-12-01
- Marketing end
- 0000-00-00
- Substance
- AMOXICILLIN; CLAVULANIC ACID
- Active strength
- 400 mg/5mL; mg/5mL
- Pharmacologic classes
- Penicillin-class Antibacterial [EPC],Penicillins [CS],beta Lactamase Inhibitor [EPC],beta Lactamase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-1865-7 | 68071186507 | 75 mL in 1 BOTTLE (68071-1865-7) | 75 ml | 2020-01-16 | 0000-00-00 | No | No | Current |