Nadolol
- Product NDC
- 21695-800
- 11-digit product format
- 216950800
- Labeler code
- 21695
- Product ID
- 21695-800_a4fc8ec9-99c6-4739-9f71-0d9062f3ebe9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nadolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Rebel Distributors Corp
- Application
- ANDA074501
- Marketing category
- ANDA
- Marketing start
- 2008-10-01
- 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
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| c3e14ce3-3dd7-c88b-aff9-2af221ac8a37 | Product name | 9 | 20240606 |
| 8fcb295c-5817-6981-e90d-9999d4e8f347 | Product name | 1 | 20140508 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 21695-800-30 | 2019-09-24 | C162847 | 48780-1 | 934fe258-4c80-48b1-e053-8cdaa90a720a | Nadolol Tablets, USP |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 21695-800-30 | Nadolol | 30 in 1 BOTTLE | TABLET | 30 | 1 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 21695-800-30 | EA - Each | 21695-800 | 78f9d068-62cf-4511-91cd-4da25521715d | 1 | 2012-07-24 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| NADOLOL | ACTIVE INGREDIENT | FEN504330V | NADOLOL TABLET [REBEL DISTRIBUTORS CORP] | 1 | |
| NADOLOL | ACTIVE MOIETY | FEN504330V | NADOLOL TABLET [REBEL DISTRIBUTORS CORP] | 1 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | NADOLOL TABLET [REBEL DISTRIBUTORS CORP] | 1 | |
| CROSCARMELLOSE SODIUM | INACTIVE INGREDIENT | M28OL1HH48 | NADOLOL TABLET [REBEL DISTRIBUTORS CORP] | 1 | |
| HYDROXYPROPYL CELLULOSE | INACTIVE INGREDIENT | RFW2ET671P | NADOLOL TABLET [REBEL DISTRIBUTORS CORP] | 1 | |
| LACTOSE MONOHYDRATE | INACTIVE INGREDIENT | EWQ57Q8I5X | NADOLOL TABLET [REBEL DISTRIBUTORS CORP] | 1 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | NADOLOL TABLET [REBEL DISTRIBUTORS CORP] | 1 | |
| SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | NADOLOL TABLET [REBEL DISTRIBUTORS CORP] | 1 | |
| STARCH, CORN | INACTIVE INGREDIENT | O8232NY3SJ | NADOLOL TABLET [REBEL DISTRIBUTORS CORP] | 1 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | NADOLOL TABLET [REBEL DISTRIBUTORS CORP] | 1 |
DailyMed Dashboard NDC Coverage#
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 198006 | nadolol 20 MG Oral Tablet | PSN | a4fc8ec9-99c6-4739-9f71-0d9062f3ebe9 | 1 |
| 198007 | nadolol 40 MG Oral Tablet | PSN | a4fc8ec9-99c6-4739-9f71-0d9062f3ebe9 | 1 |
| 198008 | nadolol 80 MG Oral Tablet | PSN | a4fc8ec9-99c6-4739-9f71-0d9062f3ebe9 | 1 |
| 198006 | nadolol 20 MG Oral Tablet | SCD | a4fc8ec9-99c6-4739-9f71-0d9062f3ebe9 | 1 |
| 198007 | nadolol 40 MG Oral Tablet | SCD | a4fc8ec9-99c6-4739-9f71-0d9062f3ebe9 | 1 |
| 198008 | nadolol 80 MG Oral Tablet | SCD | a4fc8ec9-99c6-4739-9f71-0d9062f3ebe9 | 1 |
Packages#
| Package NDC | 11-digit format | Description | Status |
|---|---|---|---|
| 21695-800-30 | 21695080030 | 30 in 1 BOTTLE | Historical |