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ACETAMINOPHEN, BUTALBITAL AND CAFFEINE
ACETAMINOPHEN, BUTALBITAL AND CAFFEINE - 16590-022-99 - (ACETAMINOPHEN, BUTALBITAL AND CAFFEINE)
Drug Information of ACETAMINOPHEN, BUTALBITAL AND CAFFEINE
| Product NDC: | 16590-022 |
| Proprietary Name: | ACETAMINOPHEN, BUTALBITAL AND CAFFEINE |
| Non Proprietary Name: | ACETAMINOPHEN, BUTALBITAL AND CAFFEINE |
| Active Ingredient(s): | 325; 50; 40 mg/1; mg/1; mg/1 & nbsp; ACETAMINOPHEN, BUTALBITAL AND CAFFEINE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ACETAMINOPHEN, BUTALBITAL AND CAFFEINE
| Product NDC: | 16590-022 |
| Labeler Name: | STAT RX USA LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA089536 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19880216 |
Package Information of ACETAMINOPHEN, BUTALBITAL AND CAFFEINE
| Package NDC: | 16590-022-99 |
| Package Description: | 500 TABLET in 1 BOTTLE, PLASTIC (16590-022-99) |
NDC Information of ACETAMINOPHEN, BUTALBITAL AND CAFFEINE
| NDC Code | 16590-022-99 |
| Proprietary Name | ACETAMINOPHEN, BUTALBITAL AND CAFFEINE |
| Package Description | 500 TABLET in 1 BOTTLE, PLASTIC (16590-022-99) |
| Product NDC | 16590-022 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ACETAMINOPHEN, BUTALBITAL AND CAFFEINE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19880216 |
| Marketing Category Name | ANDA |
| Labeler Name | STAT RX USA LLC |
| 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] |
