Atenolol
- Product NDC
- 68788-7784
- 11-digit product format
- 687887784
- Labeler code
- 68788
- Product ID
- 68788-7784_9cd2402c-4cdf-4254-9ec8-adaaffd5ea55
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA073457
- Marketing category
- ANDA
- Marketing start
- 2020-10-20
- Marketing end
- 0000-00-00
- Substance
- ATENOLOL
- Active strength
- 25 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
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 | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7784-1 | 68788778401 | 100 TABLET in 1 BOTTLE, PLASTIC (68788-7784-1) | 100 tablet | 2020-10-20 | 0000-00-00 | No | No | Current |
| 68788-7784-3 | 68788778403 | 30 TABLET in 1 BOTTLE, PLASTIC (68788-7784-3) | 30 tablet | 2020-10-20 | 0000-00-00 | No | No | Current |
| 68788-7784-6 | 68788778406 | 60 TABLET in 1 BOTTLE, PLASTIC (68788-7784-6) | 60 tablet | 2020-10-20 | 0000-00-00 | No | No | Current |
| 68788-7784-9 | 68788778409 | 90 TABLET in 1 BOTTLE, PLASTIC (68788-7784-9) | 90 tablet | 2020-10-20 | 0000-00-00 | No | No | Current |