Atenolol
- Product NDC
- 72162-2324
- 11-digit product format
- 721622324
- Labeler code
- 72162
- Product ID
- 72162-2324_b0315723-06e8-4c27-a3cb-bf08f1f8f83a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA073026
- Marketing category
- ANDA
- Marketing start
- 2022-12-19
- 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 |
|---|
| 72162-2324-0 | 72162232400 | 1000 TABLET in 1 BOTTLE (72162-2324-0) | 1000 tablet | 2024-06-05 | No | No | Historical |
| 72162-2324-9 | 72162232409 | 90 TABLET in 1 BOTTLE (72162-2324-9) | 90 tablet | 2024-06-05 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Atenolol Tablets, USP | Bryant Ranch Prepack | 2024-06-05 | HUMAN PRESCRIPTION DRUG LABEL | 100 |