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Panhematin
Panhematin - 67386-701-54 - (hemin)
Drug Information of Panhematin
| Product NDC: | 67386-701 |
| Proprietary Name: | Panhematin |
| Non Proprietary Name: | hemin |
| Active Ingredient(s): | 7 mg/mL & nbsp; hemin |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Panhematin
| Product NDC: | 67386-701 |
| Labeler Name: | Lundbeck Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | BLA101246 |
| Marketing Category: | BLA |
| Start Marketing Date: | 19830720 |
Package Information of Panhematin
| Package NDC: | 67386-701-54 |
| Package Description: | 43 mL in 1 VIAL (67386-701-54) |
NDC Information of Panhematin
| NDC Code | 67386-701-54 |
| Proprietary Name | Panhematin |
| Package Description | 43 mL in 1 VIAL (67386-701-54) |
| Product NDC | 67386-701 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | hemin |
| Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19830720 |
| Marketing Category Name | BLA |
| Labeler Name | Lundbeck Inc. |
| Substance Name | HEMIN |
| Strength Number | 7 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
