Atenolol
- Product NDC
- 76413-140
- 11-digit product format
- 764130140
- Labeler code
- 76413
- Product ID
- 76413-140_f2bb49fc-3c90-4292-a5e1-a658b2ce47a7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Central Texas Community Health Centers
- Application
- ANDA074052
- Marketing category
- ANDA
- Marketing start
- 1992-05-01
- 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
- No
- Listing certified through
- 2019-12-31
- 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 |
|---|
| 76413-140-30 | Atenolol | 30 in 1 BOTTLE, PLASTIC | TABLET | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 76413-140 | ATENOLOL TABLET [CENTRAL TEXAS COMMUNITY HEALTH CENTERS] | 1 | Legacy NDC, 1 package rows | 20161214_2763b912-c927-4113-b417-3d32d6c1cccf.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 76413-140-30 | 76413014030 | 30 in 1 BOTTLE, PLASTIC | Historical |