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Fioricet with Codeine
Fioricet with Codeine - 52544-958-01 - (butalbital, acetaminophen, caffeine, and codeine phosphate)
Drug Information of Fioricet with Codeine
| Product NDC: | 52544-958 |
| Proprietary Name: | Fioricet with Codeine |
| Non Proprietary Name: | butalbital, acetaminophen, caffeine, and codeine phosphate |
| Active Ingredient(s): | 325; 50; 40; 30 mg/1; mg/1; mg/1; mg/1 & nbsp; butalbital, acetaminophen, caffeine, and codeine phosphate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Fioricet with Codeine
| Product NDC: | 52544-958 |
| Labeler Name: | Watson Pharma, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020232 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19920730 |
Package Information of Fioricet with Codeine
| Package NDC: | 52544-958-01 |
| Package Description: | 100 CAPSULE in 1 BOTTLE (52544-958-01) |
NDC Information of Fioricet with Codeine
| NDC Code | 52544-958-01 |
| Proprietary Name | Fioricet with Codeine |
| Package Description | 100 CAPSULE in 1 BOTTLE (52544-958-01) |
| Product NDC | 52544-958 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | butalbital, acetaminophen, caffeine, and codeine phosphate |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 19920730 |
| Marketing Category Name | NDA |
| Labeler Name | Watson Pharma, Inc. |
| Substance Name | ACETAMINOPHEN; BUTALBITAL; CAFFEINE; CODEINE PHOSPHATE |
| Strength Number | 325; 50; 40; 30 |
| Strength Unit | mg/1; mg/1; mg/1; mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC],Barbiturate [EPC],Barbiturates [Chemical/Ingredient],Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE],Methylxanthine [EPC],Xanthines [Chemical/Ingredient] |
