TENORMIN
- Product NDC
- 52427-430
- 11-digit product format
- 524270430
- Labeler code
- 52427
- Product ID
- 52427-430_ecd0de7b-801e-a5d6-01b7-01b89a8f3a78
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Almatica Pharma LLC
- Application
- NDA018240
- Marketing category
- NDA
- Marketing start
- 2015-04-15
- Marketing end
- 2026-09-30
- Substance
- ATENOLOL
- Active strength
- 50 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- TENORMIN
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 |
|---|
| 52427-430-90 | TENORMIN | 90 in 1 BOTTLE | TABLET | 90 | | 23 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 52427-430 | TENORMIN (ATENOLOL) TABLET [ALMATICA PHARMA LLC] | 23 | Current NDC, Legacy NDC, 1 package rows | 20241122_746db603-a6e1-4dc3-c2d8-92314419098c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 52427-430-90 | 52427043090 | 90 TABLET in 1 BOTTLE (52427-430-90) | 90 tablet | 2015-04-15 | 2026-09-30 | No | No | Current |