Amoxicillin and Clavulanate Potassium
- Product NDC
- 68071-4170
- 11-digit product format
- 680714170
- Labeler code
- 68071
- Product ID
- 68071-4170_5f4eb99a-f4a1-350d-e053-2991aa0a40d0
- 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
- 200 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record