AMLODIPINE BESYLATE
- Product NDC
- 70934-288
- 11-digit product format
- 709340288
- Labeler code
- 70934
- Product ID
- 70934-288_ae4313a4-2505-743b-e053-2995a90a986b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- AMLODIPINE BESYLATE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA078552
- Marketing category
- ANDA
- Marketing start
- 2019-02-14
- Marketing end
- 0000-00-00
- Substance
- AMLODIPINE BESYLATE
- Active strength
- 5 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 |
|---|
| 70934-288-30 | 70934028830 | 30 TABLET in 1 BOTTLE, PLASTIC (70934-288-30) | 30 tablet | 2020-01-16 | 0000-00-00 | No | No | Current |
| 70934-288-90 | 70934028890 | 90 TABLET in 1 BOTTLE, PLASTIC (70934-288-90) | 90 tablet | 2019-02-14 | 0000-00-00 | No | No | Current |