Atenolol
- Product NDC
- 50090-6935
- 11-digit product format
- 500906935
- Labeler code
- 50090
- Product ID
- 50090-6935_2bf10cc9-8492-45c1-8e7c-5e75e1c8d283
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA074056
- Marketing category
- ANDA
- Marketing start
- 2004-11-16
- Substance
- ATENOLOL
- Active strength
- 25 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 |
|---|
| 50090-6935-0 | 50090693500 | 90 TABLET in 1 BOTTLE (50090-6935-0) | 90 tablet | 2023-12-14 | No | No | Historical |