Atenolol
- Product NDC
- 42291-140
- 11-digit product format
- 422910140
- Labeler code
- 42291
- Product ID
- 42291-140_62d7b3c5-cfaf-08d3-e053-2a91aa0abb8f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- AvKARE, Inc.
- Application
- ANDA074056
- Marketing category
- ANDA
- Marketing start
- 2013-06-17
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record