Atenolol
- Product NDC
- 68788-9761
- 11-digit product format
- 687889761
- Labeler code
- 68788
- Product ID
- 68788-9761_91bc96a4-24ae-40c3-93b5-ee50e749dbad
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceutials Inc.
- Application
- ANDA073026
- Marketing category
- ANDA
- Marketing start
- 2015-08-20
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record