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Phrenilin
Phrenilin - 0187-0842-01 - (Butalbital and Acetaminophen)
Drug Information of Phrenilin
| Product NDC: | 0187-0842 |
| Proprietary Name: | Phrenilin |
| Non Proprietary Name: | Butalbital and Acetaminophen |
| Active Ingredient(s): | 325; 50 mg/1; mg/1 & nbsp; Butalbital and Acetaminophen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Phrenilin
| Product NDC: | 0187-0842 |
| Labeler Name: | Valeant Pharmaceuticals International |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA087811 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20040503 |
Package Information of Phrenilin
| Package NDC: | 0187-0842-01 |
| Package Description: | 100 TABLET in 1 BOTTLE, PLASTIC (0187-0842-01) |
NDC Information of Phrenilin
| NDC Code | 0187-0842-01 |
| Proprietary Name | Phrenilin |
| Package Description | 100 TABLET in 1 BOTTLE, PLASTIC (0187-0842-01) |
| Product NDC | 0187-0842 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Butalbital and Acetaminophen |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20040503 |
| Marketing Category Name | ANDA |
| Labeler Name | Valeant Pharmaceuticals International |
| Substance Name | ACETAMINOPHEN; BUTALBITAL |
| Strength Number | 325; 50 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Barbiturate [EPC],Barbiturates [Chemical/Ingredient] |
