AMOXICILLIN AND CLAVULANATE POTASSIUM
- Product NDC
- 55700-751
- 11-digit product format
- 557000751
- Labeler code
- 55700
- Product ID
- 55700-751_f9105fc7-446a-4987-afa4-9d07cdd163b7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin and Clavulanate Potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA204755
- Marketing category
- ANDA
- Marketing start
- 2019-05-10
- Marketing end
- 2021-10-31
- Substance
- AMOXICILLIN; CLAVULANATE POTASSIUM
- Active strength
- 875 mg/1; mg/1
- Pharmacologic classes
- Penicillin-class Antibacterial [EPC],Penicillins [CS],beta Lactamase Inhibitor [EPC],beta Lactamase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-751-20 | 55700075120 | 20 TABLET, FILM COATED in 1 BOTTLE (55700-751-20) | 2019-05-10 | 0000-00-00 | No | No | Current |