Amlodipine Besylate
- Product NDC
- 63187-326
- 11-digit product format
- 631870326
- Labeler code
- 63187
- Product ID
- 63187-326_8edfbfb9-1c06-4032-a861-01a4d9ad7a2c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amlodipine Besylate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63187-326 | AMLODIPINE BESYLATE TABLET [PROFICIENT RX LP] | 4 | Legacy NDC | 20200219_0fdb1322-d867-4182-b7d5-30c2a27893f0.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63187-326-30 | 63187032630 | 30 TABLET in 1 BOTTLE, PLASTIC (63187-326-30) | 30 tablet | 2016-04-01 | 0000-00-00 | No | No | Current |
| 63187-326-60 | 63187032660 | 60 TABLET in 1 BOTTLE, PLASTIC (63187-326-60) | 60 tablet | 2016-04-01 | 0000-00-00 | No | No | Current |
| 63187-326-90 | 63187032690 | 90 TABLET in 1 BOTTLE, PLASTIC (63187-326-90) | 90 tablet | 2016-04-01 | 0000-00-00 | No | No | Current |