Product NDC: | 33261-881 |
Proprietary Name: | Hydrocodone Bitartate and Acetaminophen |
Non Proprietary Name: | HYDROCODONE BITARTRATE, ACETAMINOPHEN |
Active Ingredient(s): | 325; 2.5 mg/1; mg/1 & nbsp; HYDROCODONE BITARTRATE, ACETAMINOPHEN |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 33261-881 |
Labeler Name: | Aidarex Pharmaceuticals LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA040846 |
Marketing Category: | ANDA |
Start Marketing Date: | 20120517 |
Package NDC: | 33261-881-02 |
Package Description: | 120 TABLET in 1 BOTTLE, PLASTIC (33261-881-02) |
NDC Code | 33261-881-02 |
Proprietary Name | Hydrocodone Bitartate and Acetaminophen |
Package Description | 120 TABLET in 1 BOTTLE, PLASTIC (33261-881-02) |
Product NDC | 33261-881 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | HYDROCODONE BITARTRATE, ACETAMINOPHEN |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20120517 |
Marketing Category Name | ANDA |
Labeler Name | Aidarex Pharmaceuticals LLC |
Substance Name | ACETAMINOPHEN; HYDROCODONE BITARTRATE |
Strength Number | 325; 2.5 |
Strength Unit | mg/1; mg/1 |
Pharmaceutical Classes | Opioid Agonist [EPC],Opioid Agonists [MoA] |