Atenolol
- Product NDC
- 68788-9236
- 11-digit product format
- 687889236
- Labeler code
- 68788
- Product ID
- 68788-9236_c3a922c0-f38e-4d08-8d43-ca374ff7bc30
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA073025
- Marketing category
- ANDA
- Marketing start
- 2014-10-09
- 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