Atenolol
- Product NDC
- 50090-0448
- 11-digit product format
- 500900448
- Labeler code
- 50090
- Product ID
- 50090-0448_3fe7f70c-5afd-4dac-af3c-a22187ac96b7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA076900
- Marketing category
- ANDA
- Marketing start
- 2005-10-08
- Marketing end
- 0000-00-00
- Substance
- ATENOLOL
- Active strength
- 100 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 50090-0448-0 | 50090044800 | 30 TABLET in 1 BOTTLE (50090-0448-0) | 30 tablet | 2016-06-29 | 0000-00-00 | No | No | Current |
| 50090-0448-3 | 50090044803 | 60 TABLET in 1 BOTTLE (50090-0448-3) | 60 tablet | 2016-06-29 | 0000-00-00 | No | No | Current |
| 50090-0448-5 | 50090044805 | 90 TABLET in 1 BOTTLE (50090-0448-5) | 90 tablet | 2016-06-29 | 0000-00-00 | No | No | Current |