NDC Code | 71406-109-05 |
Package Description | 500 TABLET in 1 BOTTLE (71406-109-05) |
Product NDC | 71406-109 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Butalbital And Acetaminophen |
Non-Proprietary Name | Butalbital And Acetaminophen |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20211007 |
Marketing Category Name | ANDA |
Application Number | ANDA214955 |
Manufacturer | AACE Pharmaceuticals, Inc. |
Substance Name | ACETAMINOPHEN; BUTALBITAL |
Strength | 300; 50 |
Strength Unit | mg/1; mg/1 |
Pharmacy Classes | Barbiturate [EPC], Barbiturates [CS] |
DEA Schedule | CIII |