Atenolol
- Product NDC
- 60760-163
- 11-digit product format
- 607600163
- Labeler code
- 60760
- Product ID
- 60760-163_78ff532f-f234-4698-e053-2a91aa0ad7c1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA076900
- Marketing category
- ANDA
- Marketing start
- 2018-01-04
- 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
- 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 |
|---|
| 60760-163-90 | 60760016390 | 90 TABLET in 1 BOTTLE, PLASTIC (60760-163-90) | 90 tablet | 2018-01-04 | 0000-00-00 | No | No | Current |