Nabumetone
- Product NDC
- 21695-230
- 11-digit product format
- 216950230
- Labeler code
- 21695
- Product ID
- 21695-230_2564fc90-9492-448e-a64f-ee569d7853e6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nabumetone
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Rebel Distributors Corp.
- Application
- ANDA078671
- Marketing category
- ANDA
- Marketing start
- 2008-03-01
- Marketing end
- 0000-00-00
- Substance
- NABUMETONE
- Active strength
- 500 mg/1
- Pharmacologic classes
- Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 21695-230-14 | Nabumetone | 14 in 1 BOTTLE | TABLET, FILM COATED | 14 | | 2 |
| 21695-230-15 | Nabumetone | 15 in 1 BOTTLE | TABLET, FILM COATED | 15 | | 2 |
| 21695-230-20 | Nabumetone | 20 in 1 BOTTLE | TABLET, FILM COATED | 20 | | 2 |
| 21695-230-30 | Nabumetone | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 2 |
| 21695-230-60 | Nabumetone | 60 in 1 BOTTLE | TABLET, FILM COATED | 60 | | 2 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| NABUMETONE | ACTIVE INGREDIENT | LW0TIW155Z | NABUMETONE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP.] | 2 | |
| NABUMETONE | ACTIVE MOIETY | LW0TIW155Z | NABUMETONE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP.] | 2 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | NABUMETONE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP.] | 2 | |
| FERRIC OXIDE RED | INACTIVE INGREDIENT | 1K09F3G675 | NABUMETONE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP.] | 2 | |
| FERRIC OXIDE YELLOW | INACTIVE INGREDIENT | EX438O2MRT | NABUMETONE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP.] | 2 | |
| HYPROMELLOSES | INACTIVE INGREDIENT | 3NXW29V3WO | NABUMETONE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP.] | 2 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | NABUMETONE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP.] | 2 | |
| POLYETHYLENE GLYCOL | INACTIVE INGREDIENT | 3WJQ0SDW1A | NABUMETONE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP.] | 2 | |
| POLYSORBATE 80 | INACTIVE INGREDIENT | 6OZP39ZG8H | NABUMETONE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP.] | 2 | |
| SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | NABUMETONE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP.] | 2 | |
| SODIUM LAURYL SULFATE | INACTIVE INGREDIENT | 368GB5141J | NABUMETONE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP.] | 2 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | NABUMETONE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP.] | 2 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 21695-230 | NABUMETONE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP.] | 2 | Legacy NDC, 5 package rows | 20110908_87028b13-0aab-4e90-b92e-6b0c54e59bbb.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 21695-230-14 | 21695023014 | 14 in 1 BOTTLE | Historical |
| 21695-230-15 | 21695023015 | 15 in 1 BOTTLE | Historical |
| 21695-230-20 | 21695023020 | 20 in 1 BOTTLE | Historical |
| 21695-230-30 | 21695023030 | 30 in 1 BOTTLE | Historical |
| 21695-230-60 | 21695023060 | 60 in 1 BOTTLE | Historical |