Amoxicillin
- Product NDC
- 50090-6791
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA204030
- Marketing category
- ANDA
- Substance
- AMOXICILLIN
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 50090-6791-0 | 150 mL in 1 BOTTLE (50090-6791-0) | 2023-11-01 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Amoxicillin | A-S Medication Solutions | 2024-05-01 | Human Prescription Drug Label | 3 |