Nadolol
- Product NDC
- 67787-349
- 11-digit product format
- 677870349
- Labeler code
- 67787
- Product ID
- 67787-349_1f70335d-208e-4e49-a891-2182e4383be5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nadolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- InvaGen Pharmaceuticals Inc.
- Application
- ANDA203455
- Marketing category
- ANDA
- Marketing start
- 2015-12-18
- Marketing end
- 0000-00-00
- Substance
- NADOLOL
- Active strength
- 80 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
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 67787-349-10 | Nadolol | 1000 in 1 BOTTLE | TABLET | 1000 | | 2 |
| 67787-349-30 | Nadolol | 30 in 1 BOTTLE | TABLET | 30 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67787-349 | NADOLOL TABLET [INVAGEN PHARMACEUTICALS INC.] | 2 | Legacy NDC, 2 package rows | 20170822_16d317c0-829a-4233-b1aa-b96348c4ca25.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 |
|---|
| 67787-349-10 | 67787034910 | 1000 TABLET in 1 BOTTLE (67787-349-10) | 1000 tablet | 2015-12-18 | 0000-00-00 | No | No | Current |
| 67787-349-30 | 67787034930 | 30 TABLET in 1 BOTTLE (67787-349-30) | 30 tablet | 2015-12-18 | 0000-00-00 | No | No | Current |