Atenolol
- Product NDC
- 50090-0514
- 11-digit product format
- 500900514
- Labeler code
- 50090
- Product ID
- 50090-0514_7c1b1174-d4a6-4ab1-9598-89f38e0a084e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA076900
- Marketing category
- ANDA
- Marketing start
- 2005-10-08
- Marketing end
- 0000-00-00
- Substance
- ATENOLOL
- Active strength
- 25 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 50090-0514-0 | 50090051400 | 30 TABLET in 1 BOTTLE (50090-0514-0) | 30 tablet | 2016-06-29 | 0000-00-00 | No | No | Current |
| 50090-0514-2 | 50090051402 | 100 TABLET in 1 BOTTLE (50090-0514-2) | 100 tablet | 2016-06-29 | 0000-00-00 | No | No | Current |
| 50090-0514-4 | 50090051404 | 200 TABLET in 1 BOTTLE (50090-0514-4) | 200 tablet | 2016-06-29 | 0000-00-00 | No | No | Current |
| 50090-0514-5 | 50090051405 | 90 TABLET in 1 BOTTLE (50090-0514-5) | 90 tablet | 2016-06-29 | 0000-00-00 | No | No | Current |
| 50090-0514-6 | 50090051406 | 60 TABLET in 1 BOTTLE (50090-0514-6) | 60 tablet | 2016-06-29 | 0000-00-00 | No | No | Current |