Atenolol
- Product NDC
- 71335-9611
- 11-digit product format
- 713359611
- Labeler code
- 71335
- Product ID
- 71335-9611_e3dbc655-1c9c-4c0f-a95b-899198dbad58
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA213136
- Marketing category
- ANDA
- Marketing start
- 2019-11-21
- 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 |
|---|
| 71335-9611-1 | 71335961101 | 30 TABLET in 1 BOTTLE (71335-9611-1) | 30 tablet | 2022-12-19 | No | No | Historical |
| 71335-9611-2 | 71335961102 | 100 TABLET in 1 BOTTLE (71335-9611-2) | 100 tablet | 2023-02-06 | No | No | Historical |
| 71335-9611-3 | 71335961103 | 60 TABLET in 1 BOTTLE (71335-9611-3) | 60 tablet | 2024-04-03 | No | No | Historical |
| 71335-9611-4 | 71335961104 | 90 TABLET in 1 BOTTLE (71335-9611-4) | 90 tablet | 2023-01-03 | No | No | Historical |
| 71335-9611-5 | 71335961105 | 20 TABLET in 1 BOTTLE (71335-9611-5) | 20 tablet | 2024-04-03 | No | No | Historical |
| 71335-9611-6 | 71335961106 | 180 TABLET in 1 BOTTLE (71335-9611-6) | 180 tablet | 2024-04-03 | No | No | Historical |
| 71335-9611-7 | 71335961107 | 10 TABLET in 1 BOTTLE (71335-9611-7) | 10 tablet | 2024-04-03 | No | No | Historical |