Product NDC: | 0517-0375 |
Proprietary Name: | Indigo Carmine |
Non Proprietary Name: | Indigo Carmine |
Active Ingredient(s): | 8 mg/mL & nbsp; Indigo Carmine |
Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0517-0375 |
Labeler Name: | American Regent, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 19900930 |
Package NDC: | 0517-0375-10 |
Package Description: | 10 AMPULE in 1 BOX (0517-0375-10) > 5 mL in 1 AMPULE |
NDC Code | 0517-0375-10 |
Proprietary Name | Indigo Carmine |
Package Description | 10 AMPULE in 1 BOX (0517-0375-10) > 5 mL in 1 AMPULE |
Product NDC | 0517-0375 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Indigo Carmine |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAMUSCULAR; INTRAVENOUS |
Start Marketing Date | 19900930 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | American Regent, Inc. |
Substance Name | INDIGOTINDISULFONATE SODIUM |
Strength Number | 8 |
Strength Unit | mg/mL |
Pharmaceutical Classes |