Atenolol
- Product NDC
- 16571-441
- 11-digit product format
- 165710441
- Labeler code
- 16571
- Product ID
- 16571-441_d5072024-c824-4740-93af-02340db518ff
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Pack Pharmaceuticals LLC
- Application
- ANDA077443
- Marketing category
- ANDA
- Marketing start
- 2010-06-10
- 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
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#