Nadolol
- Product NDC
- 0378-0028
- 11-digit product format
- 003780028
- Labeler code
- 0378
- Product ID
- 0378-0028_5921734e-f082-4884-8e93-bce6908c69d9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- nadolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Mylan Pharmaceuticals Inc.
- Application
- ANDA074172
- Marketing category
- ANDA
- Marketing start
- 1993-10-31
- Marketing end
- 2023-11-30
- Substance
- NADOLOL
- Active strength
- 20 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| NADOLOL | ACTIVE INGREDIENT | FEN504330V | NADOLOL TABLET [PHYSICIANS TOTAL CARE, INC.] | 4 | |
| NADOLOL | ACTIVE MOIETY | FEN504330V | NADOLOL TABLET [PHYSICIANS TOTAL CARE, INC.] | 4 | |
| ANHYDROUS LACTOSE | INACTIVE INGREDIENT | 3SY5LH9PMK | NADOLOL TABLET [PHYSICIANS TOTAL CARE, INC.] | 4 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | NADOLOL TABLET [PHYSICIANS TOTAL CARE, INC.] | 4 | |
| CROSCARMELLOSE SODIUM | INACTIVE INGREDIENT | M28OL1HH48 | NADOLOL TABLET [PHYSICIANS TOTAL CARE, INC.] | 4 | |
| D&C YELLOW NO. 10 | INACTIVE INGREDIENT | 35SW5USQ3G | NADOLOL TABLET [PHYSICIANS TOTAL CARE, INC.] | 4 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | NADOLOL TABLET [PHYSICIANS TOTAL CARE, INC.] | 4 | |
| SODIUM LAURYL SULFATE | INACTIVE INGREDIENT | 368GB5141J | NADOLOL TABLET [PHYSICIANS TOTAL CARE, INC.] | 4 | |
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 |
|---|
| 0378-0028-01 | 00378002801 | 100 TABLET in 1 BOTTLE (0378-0028-01) | 100 tablet | 1993-10-31 | 0000-00-00 | No | No | Current |