Atenolol
- Product NDC
- 55289-228
- 11-digit product format
- 552890228
- Labeler code
- 55289
- Product ID
- 55289-228_7abb10c8-6c02-3c54-e053-2a91aa0a9886
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA077877
- Marketing category
- ANDA
- Marketing start
- 2007-12-04
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 55289-228-01 | EA - Each | 55289-228 | f33d6cb0-cba9-4bff-a1d4-dcf4b167fcf0 | 1 | 2012-07-24 |
| 55289-228-03 | EA - Each | 55289-228 | e0e42f45-8237-4a2e-b321-b072dd549d78 | 1 | 2012-07-24 |
| 55289-228-06 | EA - Each | 55289-228 | 46b5cac7-036c-4d61-acfb-2241dfb2c744 | 1 | 2012-07-24 |
| 55289-228-14 | EA - Each | 55289-228 | 5b431b2a-c171-4913-a8ed-72bfd6f8e5d9 | 1 | 2012-07-24 |
| 55289-228-30 | EA - Each | 55289-228 | f011c92a-08cb-48f0-b730-202e9d9412f2 | 1 | 2012-07-24 |
| 55289-228-60 | EA - Each | 55289-228 | ebc5e5fb-78f6-4a32-ba5c-cd491424a25c | 1 | 2012-07-24 |
| 55289-228-90 | EA - Each | 55289-228 | f6475edf-e74d-4c01-b1ee-84a6077d6171 | 1 | 2012-07-24 |