Nadolol
- Product NDC
- 60687-313
- 11-digit product format
- 606870313
- Labeler code
- 60687
- Product ID
- 60687-313_e0dca90d-9f91-3c1a-e053-2a95a90a6f79
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nadolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA203455
- Marketing category
- ANDA
- Marketing start
- 2017-04-15
- Marketing end
- 0000-00-00
- Substance
- NADOLOL
- Active strength
- 40 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
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 60687-313-25 | Nadolol | 30 in 1 BOX, UNIT-DOSE | TABLET | 30 | | 7 |
| 60687-313-95 | Nadolol | 1 in 1 BLISTER PACK | TABLET | 1 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60687-313 | NADOLOL TABLET [AMERICAN HEALTH PACKAGING] | 6 | Legacy NDC, 2 package rows | 20250221_9e8e129d-cb17-45fc-b3e2-2600c0166463.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60687-313-25 | 60687031325 | 30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-313-25) > 1 TABLET in 1 BLISTER PACK (60687-313-95) | 30 blister pack | 2017-04-15 | 0000-00-00 | No | No | Current |
| 60687-313-95 | 60687031395 | 1 in 1 BLISTER PACK | | | | | | Historical |