Atenolol
- Product NDC
- 50090-5233
- 11-digit product format
- 500905233
- Labeler code
- 50090
- Product ID
- 50090-5233_1da0ea2a-3f7c-4ed1-b31d-bb90847c63ec
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA073457
- Marketing category
- ANDA
- Marketing start
- 1992-01-24
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-5233 | ATENOLOL TABLET [A-S MEDICATION SOLUTIONS] | 2 | Legacy NDC, 5 package rows | 20201013_22954ed9-fbe0-42fa-a22f-6461f3f40ed5.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 |
|---|
| 50090-5233-0 | 50090523300 | 100 TABLET in 1 BOTTLE (50090-5233-0) | 100 tablet | 2020-10-09 | 0000-00-00 | No | No | Current |
| 50090-5233-1 | 50090523301 | 30 TABLET in 1 BOTTLE (50090-5233-1) | 30 tablet | 2020-10-09 | 0000-00-00 | No | No | Current |
| 50090-5233-4 | 50090523304 | 60 TABLET in 1 BOTTLE (50090-5233-4) | 60 tablet | 2020-10-09 | 0000-00-00 | No | No | Current |
| 50090-5233-7 | 50090523307 | 200 TABLET in 1 BOTTLE (50090-5233-7) | 200 tablet | 2020-10-09 | 0000-00-00 | No | No | Current |
| 50090-5233-8 | 50090523308 | 90 TABLET in 1 BOTTLE (50090-5233-8) | 90 tablet | 2020-10-09 | 0000-00-00 | No | No | Current |