| NDC Code: |
46672-059 |
| Proprietary Name: |
butalbital, acetaminophen and caffeine |
| Suffix: |
|
| Non-Proprietary Name: |
butalbital, acetaminophen and caffeine |
| Dosage Form: |
TABLET |
| Method: |
ORAL |
| Original Marketing Date: |
23-05-1988 |
| Category Name: |
ANDA |
| Application Number: |
ANDA089451 |
| Labeler: |
MIKART, INC. |
| Substance Name: |
ACETAMINOPHEN; BUTALBITAL; CAFFEINE |
| Active Numerator Strength: |
500; 50; 40 |
| Active Ingredient Unit: |
mg/1; mg/1; mg/1 |
| Pharm Classes: |
Barbiturate [EPC],Barbiturates [Chemical/Ingredient],Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE],Methylxanthine [EPC],Xanthines [Chemical/Ingredient] |
| DEA Schedule: |
|
