NDC Code | 79739-7075-1 |
Package Description | 100 TABLET in 1 BOTTLE, PLASTIC (79739-7075-1) |
Product NDC | 79739-7075 |
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 | 20110823 |
Marketing Category Name | ANDA |
Application Number | ANDA090956 |
Manufacturer | LGM Pharma Solutions, LLC |
Substance Name | BUTALBITAL; ACETAMINOPHEN |
Strength | 50; 300 |
Strength Unit | mg/1; mg/1 |
Pharmacy Classes | Barbiturates [CS],Barbiturate [EPC] |
DEA Schedule | CIII |