Atenolol
- Product NDC
- 68788-6458
- 11-digit product format
- 687886458
- Labeler code
- 68788
- Product ID
- 68788-6458_32280a61-6cb0-434c-8c19-f51d8531457f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA076900
- Marketing category
- ANDA
- Marketing start
- 2016-08-17
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record