Atenolol
- Product NDC
- 63629-1785
- 11-digit product format
- 636291785
- Labeler code
- 63629
- Product ID
- 63629-1785_3467e294-ef22-4a7d-831b-54559d70784c
- 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
- 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
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 |
|---|
| 63629-1785-1 | 63629178501 | 30 TABLET in 1 BOTTLE (63629-1785-1) | 30 tablet | 2007-12-04 | 0000-00-00 | No | No | Current |
| 63629-1785-2 | 63629178502 | 100 TABLET in 1 BOTTLE (63629-1785-2) | 100 tablet | 2007-12-04 | 0000-00-00 | No | No | Current |
| 63629-1785-3 | 63629178503 | 60 TABLET in 1 BOTTLE (63629-1785-3) | 60 tablet | 2007-12-04 | 0000-00-00 | No | No | Current |
| 63629-1785-4 | 63629178504 | 90 TABLET in 1 BOTTLE (63629-1785-4) | 90 tablet | 2007-12-04 | 0000-00-00 | No | No | Current |
| 63629-1785-5 | 63629178505 | 20 TABLET in 1 BOTTLE (63629-1785-5) | 20 tablet | 2007-12-04 | 0000-00-00 | No | No | Current |
| 63629-1785-6 | 63629178506 | 180 TABLET in 1 BOTTLE (63629-1785-6) | 180 tablet | 2007-12-04 | 0000-00-00 | No | No | Current |