Atenolol
- Product NDC
- 50090-5266
- 11-digit product format
- 500905266
- Labeler code
- 50090
- Product ID
- 50090-5266_3c9027a9-c83c-4e58-8a9d-77b62d538ffb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA077443
- Marketing category
- ANDA
- Marketing start
- 2010-06-10
- Marketing end
- 0000-00-00
- Substance
- ATENOLOL
- Active strength
- 100 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 50090-5266-0 | Atenolol | 30 in 1 BOTTLE | TABLET | 30 | | 3 |
| 50090-5266-3 | Atenolol | 60 in 1 BOTTLE | TABLET | 60 | | 3 |
| 50090-5266-5 | Atenolol | 90 in 1 BOTTLE | TABLET | 90 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-5266 | ATENOLOL TABLET [A-S MEDICATION SOLUTIONS] | 3 | Legacy NDC, 3 package rows | 20210303_3b74864b-d055-4ab6-8e0f-aed17e3b0582.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 |
|---|
| 50090-5266-0 | 50090526600 | 30 TABLET in 1 BOTTLE (50090-5266-0) | 30 tablet | 2020-10-16 | 0000-00-00 | No | No | Current |
| 50090-5266-3 | 50090526603 | 60 TABLET in 1 BOTTLE (50090-5266-3) | 60 tablet | 2020-10-16 | 0000-00-00 | No | No | Current |
| 50090-5266-5 | 50090526605 | 90 TABLET in 1 BOTTLE (50090-5266-5) | 90 tablet | 2020-10-16 | 0000-00-00 | No | No | Current |