Product NDC: | 43063-363 |
Proprietary Name: | Hydrocodone Bitartrate And Acetaminophen |
Non Proprietary Name: | Hydrocodone Bitartrate And Acetaminophen |
Active Ingredient(s): | 500; 7.5 mg/1; mg/1 & nbsp; Hydrocodone Bitartrate And Acetaminophen |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 43063-363 |
Labeler Name: | PD-Rx Pharmaceuticals, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA040144 |
Marketing Category: | ANDA |
Start Marketing Date: | 19960222 |
Package NDC: | 43063-363-10 |
Package Description: | 10 TABLET in 1 BOTTLE, PLASTIC (43063-363-10) |
NDC Code | 43063-363-10 |
Proprietary Name | Hydrocodone Bitartrate And Acetaminophen |
Package Description | 10 TABLET in 1 BOTTLE, PLASTIC (43063-363-10) |
Product NDC | 43063-363 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Hydrocodone Bitartrate And Acetaminophen |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 19960222 |
Marketing Category Name | ANDA |
Labeler Name | PD-Rx Pharmaceuticals, Inc. |
Substance Name | ACETAMINOPHEN; HYDROCODONE BITARTRATE |
Strength Number | 500; 7.5 |
Strength Unit | mg/1; mg/1 |
Pharmaceutical Classes | Opioid Agonist [EPC],Opioid Agonists [MoA] |