Atenolol
- Product NDC
- 63629-2626
- 11-digit product format
- 636292626
- Labeler code
- 63629
- Product ID
- 63629-2626_616c33eb-2e98-43f0-8892-922fd4ebc982
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077877
- Marketing category
- ANDA
- Marketing start
- 2007-12-04
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-2626-1 | 63629262601 | 100 TABLET in 1 BOTTLE (63629-2626-1) | 100 tablet | 2009-01-21 | 0000-00-00 | No | No | Current |
| 63629-2626-2 | 63629262602 | 30 TABLET in 1 BOTTLE (63629-2626-2) | 30 tablet | 2009-01-21 | 0000-00-00 | No | No | Current |
| 63629-2626-3 | 63629262603 | 60 TABLET in 1 BOTTLE (63629-2626-3) | 60 tablet | 2009-01-21 | 0000-00-00 | No | No | Current |
| 63629-2626-4 | 63629262604 | 90 TABLET in 1 BOTTLE (63629-2626-4) | 90 tablet | 2009-01-21 | 0000-00-00 | No | No | Current |
| 63629-2626-5 | 63629262605 | 20 TABLET in 1 BOTTLE (63629-2626-5) | 20 tablet | 2007-12-04 | 0000-00-00 | No | No | Current |