Atenolol
- Product NDC
- 68071-3830
- 11-digit product format
- 680713830
- Labeler code
- 68071
- Product ID
- 68071-3830_42ca57a4-29af-ef76-e063-6394a90aa683
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA078512
- Marketing category
- ANDA
- Marketing start
- 2007-10-31
- Substance
- ATENOLOL
- Active strength
- 50 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 |
|---|
| 68071-3830-1 | 68071383001 | 120 TABLET in 1 BOTTLE (68071-3830-1) | 120 tablet | 2025-04-18 | No | No | Historical |
| 68071-3830-9 | 68071383009 | 90 TABLET in 1 BOTTLE (68071-3830-9) | 90 tablet | 2025-11-04 | No | No | Historical |