Product NDC: | 0121-0655 |
Proprietary Name: | Hydrocodone Bitartrate and Acetaminophen |
Non Proprietary Name: | HYDROCODONE BITARTRATE and ACETAMINOPHEN |
Active Ingredient(s): | 167; 2.5 mg/5mL; mg/5mL & nbsp; HYDROCODONE BITARTRATE and ACETAMINOPHEN |
Administration Route(s): | ORAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0121-0655 |
Labeler Name: | Pharmaceutical Associates, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA040182 |
Marketing Category: | ANDA |
Start Marketing Date: | 20110101 |
Package NDC: | 0121-0655-04 |
Package Description: | 118 mL in 1 BOTTLE (0121-0655-04) |
NDC Code | 0121-0655-04 |
Proprietary Name | Hydrocodone Bitartrate and Acetaminophen |
Package Description | 118 mL in 1 BOTTLE (0121-0655-04) |
Product NDC | 0121-0655 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | HYDROCODONE BITARTRATE and ACETAMINOPHEN |
Dosage Form Name | SOLUTION |
Route Name | ORAL |
Start Marketing Date | 20110101 |
Marketing Category Name | ANDA |
Labeler Name | Pharmaceutical Associates, Inc. |
Substance Name | ACETAMINOPHEN; HYDROCODONE BITARTRATE |
Strength Number | 167; 2.5 |
Strength Unit | mg/5mL; mg/5mL |
Pharmaceutical Classes | Opioid Agonist [EPC],Opioid Agonists [MoA] |