AMLODIPINE BESYLATE
- Product NDC
- 70518-0274
- 11-digit product format
- 705180274
- Labeler code
- 70518
- Product ID
- 70518-0274_e72803d5-54f6-5375-e053-2995a90a1d9b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- AMLODIPINE BESYLATE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA077073
- Marketing category
- ANDA
- Marketing start
- 2017-03-02
- Marketing end
- 0000-00-00
- Substance
- AMLODIPINE BESYLATE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 70518-0274-0 | 70518027400 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-0274-0) | 90 tablet | 2017-03-02 | 0000-00-00 | No | No | Current |
| 70518-0274-1 | 70518027401 | 30 TABLET in 1 BLISTER PACK (70518-0274-1) | 30 tablet | 2017-03-16 | 0000-00-00 | No | No | Current |