Amoxicillin and Clavulanate Potassium
- Product NDC
- 68788-8956
- 11-digit product format
- 687888956
- Labeler code
- 68788
- Product ID
- 68788-8956_9db43401-cc49-4867-9e6d-e2164efeda80
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin and Clavulanate Potassium
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA065358
- Marketing category
- ANDA
- Marketing start
- 2016-01-04
- Marketing end
- 0000-00-00
- Substance
- AMOXICILLIN; CLAVULANATE POTASSIUM
- Active strength
- 600 mg/5mL; mg/5mL
- Pharmacologic classes
- beta Lactamase Inhibitor [EPC],beta Lactamase Inhibitors [MoA],Penicillin-class Antibacterial [EPC],Penicillins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record