Product NDC: | 21695-634 |
Proprietary Name: | Pentazocine HCl and Acetaminophen |
Non Proprietary Name: | Pentazocine Hydrochloride and Acetaminophen |
Active Ingredient(s): | 650; 25 mg/1; mg/1 & nbsp; Pentazocine Hydrochloride and Acetaminophen |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 21695-634 |
Labeler Name: | Rebel Distributors Corp |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA074699 |
Marketing Category: | ANDA |
Start Marketing Date: | 20000324 |
Package NDC: | 21695-634-60 |
Package Description: | 60 TABLET in 1 BOTTLE (21695-634-60) |
NDC Code | 21695-634-60 |
Proprietary Name | Pentazocine HCl and Acetaminophen |
Package Description | 60 TABLET in 1 BOTTLE (21695-634-60) |
Product NDC | 21695-634 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Pentazocine Hydrochloride and Acetaminophen |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20000324 |
Marketing Category Name | ANDA |
Labeler Name | Rebel Distributors Corp |
Substance Name | ACETAMINOPHEN; PENTAZOCINE HYDROCHLORIDE |
Strength Number | 650; 25 |
Strength Unit | mg/1; mg/1 |
Pharmaceutical Classes | Competitive Opioid Antagonists [MoA],Partial Opioid Agonist/Antagonist [EPC],Partial Opioid Agonists [MoA] |