Amoxicillin
- Product NDC
- 71205-775
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA065334
- Marketing category
- ANDA
- Substance
- AMOXICILLIN
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 71205-775-00 | 100 mL in 1 BOTTLE (71205-775-00) | 2023-03-15 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Amoxicillin | Proficient Rx LP | 2023-03-01 | HUMAN PRESCRIPTION DRUG LABEL | 1 |