Product NDC: | 49349-994 |
Proprietary Name: | Hydrocodone Bitartrate And Acetaminophen |
Non Proprietary Name: | Hydrocodone Bitartrate And Acetaminophen |
Active Ingredient(s): | 5 mg/1 & nbsp; Hydrocodone Bitartrate And Acetaminophen |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49349-994 |
Labeler Name: | REMEDYREPACK INC. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA040144 |
Marketing Category: | ANDA |
Start Marketing Date: | 20130220 |
Package NDC: | 49349-994-07 |
Package Description: | 12 TABLET in 1 BLISTER PACK (49349-994-07) |
NDC Code | 49349-994-07 |
Proprietary Name | Hydrocodone Bitartrate And Acetaminophen |
Package Description | 12 TABLET in 1 BLISTER PACK (49349-994-07) |
Product NDC | 49349-994 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Hydrocodone Bitartrate And Acetaminophen |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20130220 |
Marketing Category Name | ANDA |
Labeler Name | REMEDYREPACK INC. |
Substance Name | HYDROCODONE BITARTRATE |
Strength Number | 5 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Opioid Agonist [EPC],Opioid Agonists [MoA] |