TENORMIN
- Product NDC
- 24979-245
- 11-digit product format
- 249790245
- Labeler code
- 24979
- Product ID
- 24979-245_c804fa73-5b5a-4e20-a1f5-6a13155df21f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Upsher-Smith Laboratories, LLC
- Application
- NDA018240
- Marketing category
- NDA
- Marketing start
- 2024-08-01
- Substance
- ATENOLOL
- Active strength
- 50 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- TENORMIN
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ATENOLOL | 50 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 50VV3VW0TI |
| Rxcui | 150750, 152414, 197379, 197380, 197381, 201322 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 24979-245-07 | TENORMIN | 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 |
|---|
| 24979-245 | TENORMIN (ATENOLOL) TABLET [UPSHER-SMITH LABORATORIES, LLC] | 1 | Current NDC, 1 package rows | 20250204_6e850b1e-28a4-4ff8-8ed7-bb0b29faa28a.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 24979-245-07 | 24979024507 | 90 TABLET in 1 BOTTLE (24979-245-07) | 90 tablet | 2024-08-01 | No | No | Current |