Atenolol
- Product NDC
- 68788-6969
- 11-digit product format
- 687886969
- Labeler code
- 68788
- Product ID
- 68788-6969_b159c2e9-3d67-48ca-83cc-1a65f8b8a291
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA076900
- Marketing category
- ANDA
- Marketing start
- 2017-05-18
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-6969-1 | 68788696901 | 100 TABLET in 1 BOTTLE (68788-6969-1) | 100 tablet | 2017-05-18 | 0000-00-00 | No | No | Current |
| 68788-6969-3 | 68788696903 | 30 TABLET in 1 BOTTLE (68788-6969-3) | 30 tablet | 2017-05-18 | 0000-00-00 | No | No | Current |
| 68788-6969-6 | 68788696906 | 60 TABLET in 1 BOTTLE (68788-6969-6) | 60 tablet | 2017-05-18 | 0000-00-00 | No | No | Current |
| 68788-6969-9 | 68788696909 | 90 TABLET in 1 BOTTLE (68788-6969-9) | 90 tablet | 2017-05-18 | 0000-00-00 | No | No | Current |