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butalbital, acetaminophen and caffeine
butalbital, acetaminophen and caffeine - 68788-9711-2 - (butalbital, acetaminophen and caffeine)
Drug Information of butalbital, acetaminophen and caffeine
| Product NDC: | 68788-9711 |
| Proprietary Name: | butalbital, acetaminophen and caffeine |
| Non Proprietary Name: | butalbital, acetaminophen and caffeine |
| Active Ingredient(s): | 325; 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: | 68788-9711 |
| Labeler Name: | Preferred Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA089175 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130130 |
Package Information of butalbital, acetaminophen and caffeine
| Package NDC: | 68788-9711-2 |
| Package Description: | 20 TABLET in 1 BOTTLE (68788-9711-2) |
NDC Information of butalbital, acetaminophen and caffeine
| NDC Code | 68788-9711-2 |
| Proprietary Name | butalbital, acetaminophen and caffeine |
| Package Description | 20 TABLET in 1 BOTTLE (68788-9711-2) |
| Product NDC | 68788-9711 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | butalbital, acetaminophen and caffeine |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20130130 |
| Marketing Category Name | ANDA |
| Labeler Name | Preferred Pharmaceuticals, Inc. |
| Substance Name | ACETAMINOPHEN; BUTALBITAL; CAFFEINE |
| Strength Number | 325; 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] |
