Atenolol
- Product NDC
- 55700-755
- 11-digit product format
- 557000755
- Labeler code
- 55700
- Product ID
- 55700-755_e32b9498-9ec6-4c72-a62e-abfb41746525
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA077443
- Marketing category
- ANDA
- Marketing start
- 2019-05-17
- 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
- 2023-12-31
- 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 |
|---|
| 55700-755-30 | 55700075530 | 30 TABLET in 1 BOTTLE (55700-755-30) | 30 tablet | 2019-05-17 | 0000-00-00 | No | No | Current |