| 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 |