AMOXICILLIN AND CLAVULANATE POTASSIUM
- Product NDC
- 70518-2082
- 11-digit product format
- 705182082
- Labeler code
- 70518
- Product ID
- 70518-2082_972096e7-3315-7d80-e053-2995a90aee29
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- AMOXICILLIN AND CLAVULANATE POTASSIUM
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- NDA050725
- Marketing category
- NDA
- Marketing start
- 2019-05-15
- Marketing end
- 0000-00-00
- Substance
- AMOXICILLIN; CLAVULANATE POTASSIUM
- Active strength
- 250 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