Atenolol
- Product NDC
- 50090-3043
- 11-digit product format
- 500903043
- Labeler code
- 50090
- Product ID
- 50090-3043_9a33f5f7-fbd1-4e32-976c-eca0271c3270
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA074056
- Marketing category
- ANDA
- Marketing start
- 1995-02-22
- Marketing end
- 0000-00-00
- Substance
- ATENOLOL
- Active strength
- 50 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 50VV3VW0TI | ATENOLOL | 29122-68-7 | ATENOLOL |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-3043-0 | 50090304300 | 100 TABLET in 1 BOTTLE (50090-3043-0) | 100 tablet | 2017-06-13 | 0000-00-00 | No | No | Current |
| 50090-3043-1 | 50090304301 | 30 TABLET in 1 BOTTLE (50090-3043-1) | 30 tablet | 2017-08-02 | 0000-00-00 | No | No | Current |
| 50090-3043-4 | 50090304304 | 60 TABLET in 1 BOTTLE, PLASTIC (50090-3043-4) | 60 tablet | 2014-11-28 | 0000-00-00 | No | No | Current |
| 50090-3043-7 | 50090304307 | 200 TABLET in 1 BOTTLE (50090-3043-7) | 200 tablet | 2018-03-22 | 0000-00-00 | No | No | Current |
| 50090-3043-8 | 50090304308 | 90 TABLET in 1 BOTTLE (50090-3043-8) | 90 tablet | 2017-06-08 | 0000-00-00 | No | No | Current |