Amlodipine Besylate
- Product NDC
- 50090-5049
- 11-digit product format
- 500905049
- Labeler code
- 50090
- Product ID
- 50090-5049_6b66e014-18d2-41cd-ad4f-79be30feaea9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amlodipine Besylate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA078226
- Marketing category
- ANDA
- Marketing start
- 2007-09-21
- 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
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-5049-0 | Amlodipine Besylate | 1 in 1 BLISTER PACK | TABLET | 1 | | 1 |
| 50090-5049-0 | Amlodipine Besylate | 33 in 1 CARTON | TABLET | 33 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-5049 | AMLODIPINE BESYLATE TABLET [A-S MEDICATION SOLUTIONS] | 1 | Legacy NDC, 2 package rows | 20200725_5c347178-5cb3-40e6-8840-717c061389ed.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-5049-0 | 50090504900 | 33 BLISTER PACK in 1 CARTON (50090-5049-0) > 1 TABLET in 1 BLISTER PACK | 33 blister pack | 2020-05-15 | 0000-00-00 | No | No | Current |