Atenolol
- Product NDC
- 71335-1616
- 11-digit product format
- 713351616
- Labeler code
- 71335
- Product ID
- 71335-1616_984af795-bb5a-4156-b2cd-09707d12b5a2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- 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 |
|---|
| 71335-1616-1 | 71335161601 | 30 TABLET in 1 BOTTLE (71335-1616-1) | 30 tablet | 2004-11-16 | No | No | Historical |
| 71335-1616-2 | 71335161602 | 100 TABLET in 1 BOTTLE (71335-1616-2) | 100 tablet | 2004-11-16 | No | No | Historical |
| 71335-1616-3 | 71335161603 | 60 TABLET in 1 BOTTLE (71335-1616-3) | 60 tablet | 2004-11-16 | No | No | Historical |
| 71335-1616-4 | 71335161604 | 90 TABLET in 1 BOTTLE (71335-1616-4) | 90 tablet | 2004-11-16 | No | No | Historical |
| 71335-1616-5 | 71335161605 | 20 TABLET in 1 BOTTLE (71335-1616-5) | 20 tablet | 2004-11-16 | No | No | Historical |
| 71335-1616-6 | 71335161606 | 180 TABLET in 1 BOTTLE (71335-1616-6) | 180 tablet | 2004-11-16 | No | No | Historical |