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INDIGO CARMINE
INDIGO CARMINE - 17478-508-01 - (Indigotindisulfonate Sodium)
Drug Information of INDIGO CARMINE
| Product NDC: | 17478-508 |
| Proprietary Name: | INDIGO CARMINE |
| Non Proprietary Name: | Indigotindisulfonate Sodium |
| Active Ingredient(s): | 8 mg/mL & nbsp; Indigotindisulfonate Sodium |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of INDIGO CARMINE
| Product NDC: | 17478-508 |
| Labeler Name: | Akorn, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20090401 |
Package Information of INDIGO CARMINE
| Package NDC: | 17478-508-01 |
| Package Description: | 10 AMPULE in 1 BOX (17478-508-01) > 5 mL in 1 AMPULE |
NDC Information of INDIGO CARMINE
| NDC Code | 17478-508-01 |
| Proprietary Name | INDIGO CARMINE |
| Package Description | 10 AMPULE in 1 BOX (17478-508-01) > 5 mL in 1 AMPULE |
| Product NDC | 17478-508 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Indigotindisulfonate Sodium |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 20090401 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Akorn, Inc. |
| Substance Name | INDIGOTINDISULFONATE SODIUM |
| Strength Number | 8 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
