Amlodipine Besylate
- Product NDC
- 55700-738
- 11-digit product format
- 557000738
- Labeler code
- 55700
- Product ID
- 55700-738_2722008b-12a7-4e71-b259-74589d90d892
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amlodipine besylate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA078925
- Marketing category
- ANDA
- Marketing start
- 2019-03-29
- Marketing end
- 0000-00-00
- Substance
- AMLODIPINE BESYLATE
- Active strength
- 3 mg/1
- Pharmacologic classes
- Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 55700-738-30 | 55700073830 | 30 TABLET in 1 BOTTLE (55700-738-30) | 30 tablet | 2019-03-29 | 0000-00-00 | No | No | Current |