Amlodipine Besylate
- Product NDC
- 71205-488
- 11-digit product format
- 712050488
- Labeler code
- 71205
- Product ID
- 71205-488_9f327d08-7661-4088-b554-2f9a99a113e7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amlodipine besylate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA078925
- Marketing category
- ANDA
- Marketing start
- 2010-10-20
- 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
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 864V2Q084H | AMLODIPINE BESYLATE | 111470-99-6 | AMLODIPINE BESYLATE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71205-488-30 | 71205048830 | 30 TABLET in 1 BOTTLE (71205-488-30) | 30 tablet | 2020-10-15 | No | No | Historical |
| 71205-488-60 | 71205048860 | 60 TABLET in 1 BOTTLE (71205-488-60) | 60 tablet | 2020-10-15 | No | No | Historical |
| 71205-488-90 | 71205048890 | 90 TABLET in 1 BOTTLE (71205-488-90) | 90 tablet | 2020-10-15 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Amlodipine Besylate | Proficient Rx LP | 2020-10-01 | HUMAN PRESCRIPTION DRUG LABEL | 1 |