Amlodipine Besylate
- Product NDC
- 60760-459
- 11-digit product format
- 607600459
- Labeler code
- 60760
- Product ID
- 60760-459_a500b8fb-e32a-632d-e053-2a95a90ac22f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amlodipine Besylate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA203245
- Marketing category
- ANDA
- Marketing start
- 2020-05-06
- Marketing end
- 0000-00-00
- Substance
- AMLODIPINE BESYLATE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60760-459-30 | 60760045930 | 30 TABLET in 1 BOTTLE, PLASTIC (60760-459-30) | 30 tablet | 2020-05-06 | 0000-00-00 | No | No | Current |
| 60760-459-90 | 60760045990 | 90 TABLET in 1 BOTTLE, PLASTIC (60760-459-90) | 90 tablet | 2020-05-06 | 0000-00-00 | No | No | Current |