Atenolol
- Product NDC
- 71335-1355
- 11-digit product format
- 713351355
- Labeler code
- 71335
- Product ID
- 71335-1355_7fc7bc39-bd19-4063-8961-83856175688b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA073025
- Marketing category
- ANDA
- Marketing start
- 1991-09-17
- Marketing end
- 0000-00-00
- Substance
- ATENOLOL
- Active strength
- 50 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 |
|---|
| 71335-1355-1 | 71335135501 | 30 TABLET in 1 BOTTLE (71335-1355-1) | 30 tablet | 2009-05-26 | 0000-00-00 | No | No | Current |
| 71335-1355-2 | 71335135502 | 100 TABLET in 1 BOTTLE (71335-1355-2) | 100 tablet | 2009-05-26 | 0000-00-00 | No | No | Current |
| 71335-1355-3 | 71335135503 | 60 TABLET in 1 BOTTLE (71335-1355-3) | 60 tablet | 2009-05-26 | 0000-00-00 | No | No | Current |
| 71335-1355-4 | 71335135504 | 90 TABLET in 1 BOTTLE (71335-1355-4) | 90 tablet | 2009-05-26 | 0000-00-00 | No | No | Current |
| 71335-1355-5 | 71335135505 | 20 TABLET in 1 BOTTLE (71335-1355-5) | 20 tablet | 2009-05-26 | 0000-00-00 | No | No | Current |
| 71335-1355-6 | 71335135506 | 10 TABLET in 1 BOTTLE (71335-1355-6) | 10 tablet | 2009-05-26 | 0000-00-00 | No | No | Current |