Atenolol
- Product NDC
- 50090-3410
- 11-digit product format
- 500903410
- Labeler code
- 50090
- Product ID
- 50090-3410_f0b4e8cf-2285-4510-bcc1-5282e147beb9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA074056
- Marketing category
- ANDA
- Marketing start
- 1995-02-17
- Marketing end
- 0000-00-00
- Substance
- ATENOLOL
- Active strength
- 100 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 |
|---|
| 50090-3410-0 | 50090341000 | 30 TABLET in 1 BOTTLE, PLASTIC (50090-3410-0) | 30 tablet | 2014-11-28 | 0000-00-00 | No | No | Current |
| 50090-3410-1 | 50090341001 | 3 TABLET in 1 BOTTLE (50090-3410-1) | 3 tablet | 2019-01-31 | 0000-00-00 | No | No | Current |
| 50090-3410-3 | 50090341003 | 60 TABLET in 1 BOTTLE (50090-3410-3) | 60 tablet | 2018-03-30 | 0000-00-00 | No | No | Current |
| 50090-3410-5 | 50090341005 | 90 TABLET in 1 BOTTLE (50090-3410-5) | 90 tablet | 2018-03-22 | 0000-00-00 | No | No | Current |