Nadolol
- Product NDC
- 71335-1972
- 11-digit product format
- 713351972
- Labeler code
- 71335
- Product ID
- 71335-1972_a8ecc34e-d850-42d9-8dde-99cc268ef573
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nadolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA074255
- Marketing category
- ANDA
- Marketing start
- 2020-07-10
- 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
- 2022-12-31
- 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 |
|---|
| 71335-1972-1 | Nadolol | 30 in 1 BOTTLE | TABLET | 30 | | 100 |
| 71335-1972-2 | Nadolol | 28 in 1 BOTTLE | TABLET | 28 | | 100 |
| 71335-1972-3 | Nadolol | 90 in 1 BOTTLE | TABLET | 90 | | 100 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71335-1972 | NADOLOL TABLET [BRYANT RANCH PREPACK] | 100 | Legacy NDC, 3 package rows | 20211023_efc27b02-693b-4719-821b-e2a551552777.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 |
|---|
| 71335-1972-1 | 71335197201 | 30 TABLET in 1 BOTTLE (71335-1972-1) | 30 tablet | 2021-10-21 | 0000-00-00 | No | No | Current |
| 71335-1972-2 | 71335197202 | 28 TABLET in 1 BOTTLE (71335-1972-2) | 28 tablet | 2021-10-21 | 0000-00-00 | No | No | Current |
| 71335-1972-3 | 71335197203 | 90 TABLET in 1 BOTTLE (71335-1972-3) | 90 tablet | 2021-10-21 | 0000-00-00 | No | No | Current |