Home
>
National Drug Code (NDC)
>
Vicoprofen
Vicoprofen - 0074-2277-12 - (Hydrocodone Bitartrate and Ibuprofen)
Drug Information of Vicoprofen
| Product NDC: | 0074-2277 |
| Proprietary Name: | Vicoprofen |
| 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, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Vicoprofen
| Product NDC: | 0074-2277 |
| Labeler Name: | Abbott Laboratories |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020716 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19970923 |
Package Information of Vicoprofen
| Package NDC: | 0074-2277-12 |
| Package Description: | 4 BLISTER PACK in 1 CARTON (0074-2277-12) > 25 TABLET, COATED in 1 BLISTER PACK |
NDC Information of Vicoprofen
| NDC Code | 0074-2277-12 |
| Proprietary Name | Vicoprofen |
| Package Description | 4 BLISTER PACK in 1 CARTON (0074-2277-12) > 25 TABLET, COATED in 1 BLISTER PACK |
| Product NDC | 0074-2277 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Hydrocodone Bitartrate and Ibuprofen |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 19970923 |
| Marketing Category Name | NDA |
| Labeler Name | Abbott Laboratories |
| 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] |
