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Hydrocodone Bitartrate and Ibuprofen
Hydrocodone Bitartrate and Ibuprofen - 63739-557-10 - (Hydrocodone Bitartrate and Ibuprofen)
Drug Information of Hydrocodone Bitartrate and Ibuprofen
| Product NDC: | 63739-557 |
| 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 |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Hydrocodone Bitartrate and Ibuprofen
| Product NDC: | 63739-557 |
| Labeler Name: | McKesson Packaging Services a business unit of McKesson Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076642 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120521 |
Package Information of Hydrocodone Bitartrate and Ibuprofen
| Package NDC: | 63739-557-10 |
| Package Description: | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-557-10) > 10 TABLET in 1 BLISTER PACK |
NDC Information of Hydrocodone Bitartrate and Ibuprofen
| NDC Code | 63739-557-10 |
| Proprietary Name | Hydrocodone Bitartrate and Ibuprofen |
| Package Description | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-557-10) > 10 TABLET in 1 BLISTER PACK |
| Product NDC | 63739-557 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Hydrocodone Bitartrate and Ibuprofen |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20120521 |
| Marketing Category Name | ANDA |
| Labeler Name | McKesson Packaging Services a business unit of McKesson Corporation |
| 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] |
