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HONEY BEE VENOM
HONEY BEE VENOM - 52709-0801-1 - (APIS MELLIFERA VENOM)
Drug Information of HONEY BEE VENOM
| Product NDC: | 52709-0801 |
| Proprietary Name: | HONEY BEE VENOM |
| Non Proprietary Name: | APIS MELLIFERA VENOM |
| Active Ingredient(s): | 120 ug/1 & nbsp; APIS MELLIFERA VENOM |
| Administration Route(s): | SUBCUTANEOUS |
| Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of HONEY BEE VENOM
| Product NDC: | 52709-0801 |
| Labeler Name: | ALK-Abello A S |
| Product Type: | NON-STANDARDIZED ALLERGENIC |
| FDA Application Number: | BLA103969 |
| Marketing Category: | BLA |
| Start Marketing Date: | 19921120 |
Package Information of HONEY BEE VENOM
| Package NDC: | 52709-0801-1 |
| Package Description: | 6 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 PACKAGE (52709-0801-1) |
NDC Information of HONEY BEE VENOM
| NDC Code | 52709-0801-1 |
| Proprietary Name | HONEY BEE VENOM |
| Package Description | 6 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 PACKAGE (52709-0801-1) |
| Product NDC | 52709-0801 |
| Product Type Name | NON-STANDARDIZED ALLERGENIC |
| Non Proprietary Name | APIS MELLIFERA VENOM |
| Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route Name | SUBCUTANEOUS |
| Start Marketing Date | 19921120 |
| Marketing Category Name | BLA |
| Labeler Name | ALK-Abello A S |
| Substance Name | APIS MELLIFERA VENOM |
| Strength Number | 120 |
| Strength Unit | ug/1 |
| Pharmaceutical Classes |
