Nabumetone
- Product NDC
- 33358-252
- 11-digit product format
- 333580252
- Labeler code
- 33358
- Product ID
- 33358-252_5663a37f-b62f-4a8b-832a-33f95a4afbdc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nabumetone
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- RxChange Co.
- Application
- ANDA078671
- Marketing category
- ANDA
- Marketing start
- 2014-11-13
- Marketing end
- 0000-00-00
- Substance
- NABUMETONE
- Active strength
- 750 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 |
|---|
| 33358-252-60 | Nabumetone | 60 in 1 BOTTLE | TABLET, FILM COATED | 60 | | 1 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| NABUMETONE | ACTIVE INGREDIENT | LW0TIW155Z | NABUMETONE TABLET, FILM COATED [RXCHANGE CO.] | 1 | |
| NABUMETONE | ACTIVE MOIETY | LW0TIW155Z | NABUMETONE TABLET, FILM COATED [RXCHANGE CO.] | 1 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | NABUMETONE TABLET, FILM COATED [RXCHANGE CO.] | 1 | |
| FERRIC OXIDE RED | INACTIVE INGREDIENT | 1K09F3G675 | NABUMETONE TABLET, FILM COATED [RXCHANGE CO.] | 1 | |
| FERRIC OXIDE YELLOW | INACTIVE INGREDIENT | EX438O2MRT | NABUMETONE TABLET, FILM COATED [RXCHANGE CO.] | 1 | |
| HYPROMELLOSES | INACTIVE INGREDIENT | 3NXW29V3WO | NABUMETONE TABLET, FILM COATED [RXCHANGE CO.] | 1 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | NABUMETONE TABLET, FILM COATED [RXCHANGE CO.] | 1 | |
| POLYETHYLENE GLYCOLS | INACTIVE INGREDIENT | 3WJQ0SDW1A | NABUMETONE TABLET, FILM COATED [RXCHANGE CO.] | 1 | |
| POLYSORBATE 80 | INACTIVE INGREDIENT | 6OZP39ZG8H | NABUMETONE TABLET, FILM COATED [RXCHANGE CO.] | 1 | |
| SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | NABUMETONE TABLET, FILM COATED [RXCHANGE CO.] | 1 | |
| SODIUM LAURYL SULFATE | INACTIVE INGREDIENT | 368GB5141J | NABUMETONE TABLET, FILM COATED [RXCHANGE CO.] | 1 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | NABUMETONE TABLET, FILM COATED [RXCHANGE CO.] | 1 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 33358-252 | NABUMETONE TABLET, FILM COATED [RXCHANGE CO.] | 1 | Legacy NDC, 1 package rows | 20141114_e6a40890-d3ce-400c-a552-0d5ad28193c5.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 33358-252-60 | 33358025260 | 60 in 1 BOTTLE | Historical |