Product NDC: | 51293-617 |
Proprietary Name: | Isometheptene Mucate/Dichloralphenazone/Acetaminophen |
Non Proprietary Name: | ISOMETHEPTENE MUCATE, DICHLORALPHENAZONE, and ACETAMINOPHEN |
Active Ingredient(s): | 325; 100; 65 mg/1; mg/1; mg/1 & nbsp; ISOMETHEPTENE MUCATE, DICHLORALPHENAZONE, and ACETAMINOPHEN |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51293-617 |
Labeler Name: | ECI Pharmaceuticals LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20110215 |
Package NDC: | 51293-617-67 |
Package Description: | 50 CAPSULE in 1 BOTTLE, GLASS (51293-617-67) |
NDC Code | 51293-617-67 |
Proprietary Name | Isometheptene Mucate/Dichloralphenazone/Acetaminophen |
Package Description | 50 CAPSULE in 1 BOTTLE, GLASS (51293-617-67) |
Product NDC | 51293-617 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | ISOMETHEPTENE MUCATE, DICHLORALPHENAZONE, and ACETAMINOPHEN |
Dosage Form Name | CAPSULE |
Route Name | ORAL |
Start Marketing Date | 20110215 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | ECI Pharmaceuticals LLC |
Substance Name | ACETAMINOPHEN; DICHLORALPHENAZONE; ISOMETHEPTENE MUCATE |
Strength Number | 325; 100; 65 |
Strength Unit | mg/1; mg/1; mg/1 |
Pharmaceutical Classes |