AMLODIPINE BESYLATE
- Product NDC
- 60760-132
- 11-digit product format
- 607600132
- Labeler code
- 60760
- Product ID
- 60760-132_b674e898-4fa8-5a6b-e053-2a95a90a5b21
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- AMLODIPINE BESYLATE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA077073
- Marketing category
- ANDA
- Marketing start
- 2007-09-26
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60760-132-30 | 60760013230 | 30 TABLET in 1 BOTTLE, PLASTIC (60760-132-30) | 30 tablet | 2017-11-14 | 0000-00-00 | No | No | Current |
| 60760-132-90 | 60760013290 | 90 TABLET in 1 BOTTLE, PLASTIC (60760-132-90) | 90 tablet | 2017-11-14 | 0000-00-00 | No | No | Current |