Atenolol
- Product NDC
- 63629-6461
- 11-digit product format
- 636296461
- Labeler code
- 63629
- Product ID
- 63629-6461_49a2cd59-0f2e-4f15-872c-b98d6a1ffdea
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA073025
- Marketing category
- ANDA
- Marketing start
- 1991-09-17
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-6461-1 | 63629646101 | 30 TABLET in 1 BOTTLE (63629-6461-1) | 30 tablet | 2015-08-28 | 0000-00-00 | No | No | Current |