Amlodipine Besylate
- Product NDC
- 71610-938
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amlodipine Besylate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA076846
- Marketing category
- ANDA
- Substance
- AMLODIPINE BESYLATE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 71610-938-30 | 30 TABLET in 1 BOTTLE (71610-938-30) | 2025-08-21 | | No | Historical |
| 71610-938-45 | 45 TABLET in 1 BOTTLE (71610-938-45) | 2025-08-21 | | No | Historical |
| 71610-938-53 | 60 TABLET in 1 BOTTLE (71610-938-53) | 2025-08-21 | | No | Historical |
| 71610-938-60 | 90 TABLET in 1 BOTTLE (71610-938-60) | 2025-08-21 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Amlodipine Besylate | Aphena Pharma Solutions - Tennessee, LLC | 2025-08-21 | HUMAN PRESCRIPTION DRUG LABEL | 1 |