Atenolol
- Product NDC
- 71205-496
- 11-digit product format
- 712050496
- Labeler code
- 71205
- Product ID
- 71205-496_e115f27a-6a7c-498c-b4a1-2d4c5716af22
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA073457
- Marketing category
- ANDA
- Marketing start
- 1992-01-24
- 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 |
|---|
| 71205-496-30 | 71205049630 | 30 TABLET in 1 BOTTLE, PLASTIC (71205-496-30) | 30 tablet | 2020-10-23 | No | No | Historical |
| 71205-496-60 | 71205049660 | 60 TABLET in 1 BOTTLE, PLASTIC (71205-496-60) | 60 tablet | 2020-10-23 | No | No | Historical |
| 71205-496-90 | 71205049690 | 90 TABLET in 1 BOTTLE, PLASTIC (71205-496-90) | 90 tablet | 2020-10-23 | No | No | Historical |