Amoxicillin and Clavulanate Potassium
- Product NDC
- 59115-061
- 11-digit product format
- 591150061
- Labeler code
- 59115
- Product ID
- 59115-061_bab44f07-66d6-489a-b3db-57c235666b3a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin and Clavulanate Potassium
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- Hikma Pharmaceutical
- Application
- ANDA065373
- Marketing category
- ANDA
- Marketing start
- 2007-11-09
- Marketing end
- 0000-00-00
- Substance
- AMOXICILLIN; CLAVULANATE POTASSIUM
- Active strength
- 600 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