Norvasc
- Product NDC
- 55289-103
- 11-digit product format
- 552890103
- Labeler code
- 55289
- Product ID
- 55289-103_dcf54414-99d9-86f9-e053-2a95a90a309b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- amlodipine besylate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- NDA019787
- Marketing category
- NDA
- Marketing start
- 1992-07-31
- 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
- 2023-12-31
- 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 |
|---|
| 55289-103-30 | 55289010330 | 30 TABLET in 1 BOTTLE, PLASTIC (55289-103-30) | 30 tablet | 2011-10-17 | 0000-00-00 | No | No | Current |
| 55289-103-60 | 55289010360 | 60 TABLET in 1 BOTTLE, PLASTIC (55289-103-60) | 60 tablet | 2011-10-17 | 0000-00-00 | No | No | Current |