| 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 |