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HYDROCODONE BITARTRATE AND IBUPROFEN
HYDROCODONE BITARTRATE AND IBUPROFEN - 62037-524-01 - (HYDROCODONE BITARTRATE AND IBUPROFEN)
Drug Information of HYDROCODONE BITARTRATE AND IBUPROFEN
| Product NDC: | 62037-524 |
| Proprietary Name: | HYDROCODONE BITARTRATE AND IBUPROFEN |
| Non Proprietary Name: | HYDROCODONE BITARTRATE AND IBUPROFEN |
| Active Ingredient(s): | 7.5; 200 mg/1; mg/1 & nbsp; HYDROCODONE BITARTRATE AND IBUPROFEN |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of HYDROCODONE BITARTRATE AND IBUPROFEN
| Product NDC: | 62037-524 |
| Labeler Name: | Watson Pharma, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076604 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20040401 |
Package Information of HYDROCODONE BITARTRATE AND IBUPROFEN
| Package NDC: | 62037-524-01 |
| Package Description: | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (62037-524-01) |
NDC Information of HYDROCODONE BITARTRATE AND IBUPROFEN
| NDC Code | 62037-524-01 |
| Proprietary Name | HYDROCODONE BITARTRATE AND IBUPROFEN |
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (62037-524-01) |
| Product NDC | 62037-524 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | HYDROCODONE BITARTRATE AND IBUPROFEN |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20040401 |
| Marketing Category Name | ANDA |
| Labeler Name | Watson Pharma, Inc. |
| Substance Name | HYDROCODONE BITARTRATE; IBUPROFEN |
| Strength Number | 7.5; 200 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Opioid Agonist [EPC],Opioid Agonists [MoA],Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |
