Atenolol
- Product NDC
- 35356-930
- 11-digit product format
- 353560930
- Labeler code
- 35356
- Product ID
- 35356-930_34da6242-0058-4a6d-8a60-8cfe52b28c34
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA074052
- Marketing category
- ANDA
- Marketing start
- 1992-05-01
- Marketing end
- 0000-00-00
- Substance
- ATENOLOL
- Active strength
- 25 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