Amoxicillin and Clavulanate Potassium
- Product NDC
- 55700-538
- 11-digit product format
- 557000538
- Labeler code
- 55700
- Product ID
- 55700-538_3e4b1a47-92b7-48a4-b6a4-e4302d97755c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin and Clavulanate Potassium
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA065373
- Marketing category
- ANDA
- Marketing start
- 2009-08-03
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record