Atenolol
- Product NDC
- 55700-240
- 11-digit product format
- 557000240
- Labeler code
- 55700
- Product ID
- 55700-240_a06bb9ee-8c03-4a77-964f-c8b13d09734e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- 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 |