Amlodipine Besylate
- Product NDC
- 50090-4903
- 11-digit product format
- 500904903
- Labeler code
- 50090
- Product ID
- 50090-4903_45847676-154d-4583-a61a-4ec3b5ea9712
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amlodipine Besylate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA203245
- Marketing category
- ANDA
- Marketing start
- 2014-03-03
- Marketing end
- 0000-00-00
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-4903 | AMLODIPINE BESYLATE TABLET [A-S MEDICATION SOLUTIONS] | 3 | Legacy NDC | 20230208_f05dd8da-144c-434a-9d48-cc474a1c663d.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-4903-0 | 50090490300 | 90 TABLET in 1 BOTTLE (50090-4903-0) | 90 tablet | 2020-02-17 | 0000-00-00 | No | No | Current |