Atenolol
- Product NDC
- 43353-986
- 11-digit product format
- 433530986
- Labeler code
- 43353
- Product ID
- 43353-986_7eca20ff-75cb-402d-942a-7c4854718687
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA073457
- Marketing category
- ANDA
- Marketing start
- 2014-02-20
- Substance
- ATENOLOL
- Active strength
- 100 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 50VV3VW0TI | ATENOLOL | 29122-68-7 | ATENOLOL |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 43353-986-60 | 43353098660 | 90 TABLET in 1 BOTTLE, PLASTIC (43353-986-60) | 90 tablet | 2014-12-04 | No | No | Historical |