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Butalbital, Acetaminophen and Caffeine
Butalbital, Acetaminophen and Caffeine - 21695-257-60 - (Butalbital, Acetaminophen and Caffeine)
Drug Information of Butalbital, Acetaminophen and Caffeine
| Product NDC: | 21695-257 |
| Proprietary Name: | Butalbital, Acetaminophen and Caffeine |
| Non Proprietary Name: | Butalbital, Acetaminophen and Caffeine |
| Active Ingredient(s): | 500; 50; 40 mg/1; mg/1; mg/1 & nbsp; Butalbital, Acetaminophen and Caffeine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Butalbital, Acetaminophen and Caffeine
| Product NDC: | 21695-257 |
| Labeler Name: | Rebel Distributors Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040336 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091215 |
Package Information of Butalbital, Acetaminophen and Caffeine
| Package NDC: | 21695-257-60 |
| Package Description: | 60 TABLET in 1 BOTTLE (21695-257-60) |
NDC Information of Butalbital, Acetaminophen and Caffeine
| NDC Code | 21695-257-60 |
| Proprietary Name | Butalbital, Acetaminophen and Caffeine |
| Package Description | 60 TABLET in 1 BOTTLE (21695-257-60) |
| Product NDC | 21695-257 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Butalbital, Acetaminophen and Caffeine |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20091215 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp. |
| Substance Name | ACETAMINOPHEN; BUTALBITAL; CAFFEINE |
| Strength Number | 500; 50; 40 |
| Strength Unit | mg/1; mg/1; mg/1 |
| Pharmaceutical Classes | Barbiturate [EPC],Barbiturates [Chemical/Ingredient],Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE],Methylxanthine [EPC],Xanthines [Chemical/Ingredient] |
