Atenolol
- Product NDC
- 50090-2811
- 11-digit product format
- 500902811
- Labeler code
- 50090
- Product ID
- 50090-2811_1c530b16-6e36-4f78-9040-a3720813df50
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA073457
- Marketing category
- ANDA
- Marketing start
- 1992-01-24
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 50VV3VW0TI | ATENOLOL | 29122-68-7 | ATENOLOL |