Amlodipine besylate
- Product NDC
- 71610-722
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amlodipine besylate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA077955
- Marketing category
- ANDA
- Substance
- AMLODIPINE BESYLATE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 71610-722-15 | 15 TABLET in 1 BOTTLE (71610-722-15) | 2023-09-06 | | No | Historical |
| 71610-722-30 | 30 TABLET in 1 BOTTLE (71610-722-30) | 2023-09-06 | | No | Historical |
| 71610-722-45 | 45 TABLET in 1 BOTTLE (71610-722-45) | 2023-07-27 | | No | Historical |
| 71610-722-60 | 90 TABLET in 1 BOTTLE (71610-722-60) | 2023-07-27 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Amlodipine besylate | Aphena Pharma Solutions - Tennessee, LLC | 2023-09-07 | Human Prescription Drug Label | 3 |