Atenolol
- Product NDC
- 71335-1379
- 11-digit product format
- 713351379
- Labeler code
- 71335
- Product ID
- 71335-1379_7fc7bc39-bd19-4063-8961-83856175688b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA073026
- Marketing category
- ANDA
- Marketing start
- 1991-09-17
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-1379-1 | 71335137901 | 100 TABLET in 1 BOTTLE (71335-1379-1) | 100 tablet | 2019-10-31 | 0000-00-00 | No | No | Current |
| 71335-1379-2 | 71335137902 | 30 TABLET in 1 BOTTLE (71335-1379-2) | 30 tablet | 2019-10-31 | 0000-00-00 | No | No | Current |
| 71335-1379-3 | 71335137903 | 60 TABLET in 1 BOTTLE (71335-1379-3) | 60 tablet | 2019-10-31 | 0000-00-00 | No | No | Current |
| 71335-1379-4 | 71335137904 | 90 TABLET in 1 BOTTLE (71335-1379-4) | 90 tablet | 2019-10-31 | 0000-00-00 | No | No | Current |
| 71335-1379-5 | 71335137905 | 20 TABLET in 1 BOTTLE (71335-1379-5) | 20 tablet | 2019-10-31 | 0000-00-00 | No | No | Current |