Amoxicillin and Clavulanate Potassium
- Product NDC
- 71205-712
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin and Clavulanate Potassium
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA065063
- Marketing category
- ANDA
- Substance
- AMOXICILLIN; CLAVULANATE POTASSIUM
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 71205-712-10 | 10 TABLET, FILM COATED in 1 BOTTLE (71205-712-10) | 2022-11-15 | | No | Historical |
| 71205-712-14 | 14 TABLET, FILM COATED in 1 BOTTLE (71205-712-14) | 2022-11-15 | | No | Historical |
| 71205-712-20 | 20 TABLET, FILM COATED in 1 BOTTLE (71205-712-20) | 2022-11-15 | | No | Historical |
| 71205-712-21 | 21 TABLET, FILM COATED in 1 BOTTLE (71205-712-21) | 2022-11-15 | | No | Historical |
| 71205-712-28 | 28 TABLET, FILM COATED in 1 BOTTLE (71205-712-28) | 2022-11-15 | | No | Historical |
| 71205-712-30 | 30 TABLET, FILM COATED in 1 BOTTLE (71205-712-30) | 2022-11-15 | | No | Historical |
| 71205-712-60 | 60 TABLET, FILM COATED in 1 BOTTLE (71205-712-60) | 2022-11-15 | | No | Historical |
| 71205-712-90 | 90 TABLET, FILM COATED in 1 BOTTLE (71205-712-90) | 2022-11-15 | | No | Historical |