Amoxicillin
- Product NDC
- 68071-3675
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA065256
- Marketing category
- ANDA
- Substance
- AMOXICILLIN
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 68071-3675-2 | 20 TABLET, FILM COATED in 1 BOTTLE (68071-3675-2) | 2024-08-30 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Amoxicillin | NuCare Pharmaceuticals, Inc. | 2024-08-30 | HUMAN PRESCRIPTION DRUG LABEL | 1 |