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Nabumetone
Nabumetone - 51079-989-20 - (Nabumetone)
Drug Information of Nabumetone
| Product NDC: | 51079-989 |
| Proprietary Name: | Nabumetone |
| Non Proprietary Name: | Nabumetone |
| Active Ingredient(s): | 500 mg/1 & nbsp; Nabumetone |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Nabumetone
| Product NDC: | 51079-989 |
| Labeler Name: | UDL Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075189 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100806 |
Package Information of Nabumetone
| Package NDC: | 51079-989-20 |
| Package Description: | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-989-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-989-01) |
NDC Information of Nabumetone
| NDC Code | 51079-989-20 |
| Proprietary Name | Nabumetone |
| Package Description | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-989-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-989-01) |
| Product NDC | 51079-989 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Nabumetone |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20100806 |
| Marketing Category Name | ANDA |
| Labeler Name | UDL Laboratories, Inc. |
| Substance Name | NABUMETONE |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |
