Atenolol
- Product NDC
- 10544-167
- 11-digit product format
- 105440167
- Labeler code
- 10544
- Product ID
- 10544-167_101ced94-a656-0123-e054-00144ff8d46c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Blenheim Pharmacal, Inc.
- Application
- ANDA077443
- Marketing category
- ANDA
- Marketing start
- 2013-11-15
- 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
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 10544-167-30 | Atenolol | 30 in 1 BOTTLE | TABLET | 30 | | 2 |
| 10544-167-90 | Atenolol | 90 in 1 BOTTLE | TABLET | 90 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 10544-167 | ATENOLOL TABLET [BLENHEIM PHARMACAL, INC.] | 2 | Legacy NDC, 2 package rows | 20150228_793b6b1d-54fd-4856-ab0b-899bb046a239.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 10544-167-30 | 10544016730 | 30 in 1 BOTTLE | Historical |
| 10544-167-90 | 10544016790 | 90 in 1 BOTTLE | Historical |