Atenolol
- Product NDC
- 71610-861
- 11-digit product format
- 716100861
- Labeler code
- 71610
- Product ID
- 71610-861_247569cb-f6d8-d99c-e063-6394a90aad97
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA074056
- Marketing category
- ANDA
- Marketing start
- 1995-02-22
- Substance
- ATENOLOL
- Active strength
- 50 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 50VV3VW0TI | ATENOLOL | 29122-68-7 | ATENOLOL |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71610-861-30 | 71610086130 | 30 TABLET in 1 BOTTLE (71610-861-30) | 30 tablet | 2024-10-11 | No | No | Historical |
| 71610-861-45 | 71610086145 | 45 TABLET in 1 BOTTLE (71610-861-45) | 45 tablet | 2024-10-11 | No | No | Historical |
| 71610-861-60 | 71610086160 | 90 TABLET in 1 BOTTLE (71610-861-60) | 90 tablet | 2024-10-11 | No | No | Historical |
| 71610-861-73 | 71610086173 | 135 TABLET in 1 BOTTLE (71610-861-73) | 135 tablet | 2024-10-11 | No | No | Historical |
| 71610-861-80 | 71610086180 | 180 TABLET in 1 BOTTLE (71610-861-80) | 180 tablet | 2024-10-11 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| ATENOLOL TABLETS USP Rx only | Aphena Pharma Solutions - Tennessee, LLC | 2024-10-14 | HUMAN PRESCRIPTION DRUG LABEL | 1 |