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Glucagon
Glucagon - 0002-8031-01 - (glucagon)
Drug Information of Glucagon
| Product NDC: | 0002-8031 |
| Proprietary Name: | Glucagon |
| Non Proprietary Name: | glucagon |
| Active Ingredient(s): | & nbsp; glucagon |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Glucagon
| Product NDC: | 0002-8031 |
| Labeler Name: | Eli Lilly and Company |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020928 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19990301 |
Package Information of Glucagon
| Package NDC: | 0002-8031-01 |
| Package Description: | 1 KIT in 1 KIT (0002-8031-01) * 1 mL in 1 VIAL (0002-7529-01) * 1 mL in 1 SYRINGE (0002-7530-01) |
NDC Information of Glucagon
| NDC Code | 0002-8031-01 |
| Proprietary Name | Glucagon |
| Package Description | 1 KIT in 1 KIT (0002-8031-01) * 1 mL in 1 VIAL (0002-7529-01) * 1 mL in 1 SYRINGE (0002-7530-01) |
| Product NDC | 0002-8031 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | glucagon |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 19990301 |
| Marketing Category Name | NDA |
| Labeler Name | Eli Lilly and Company |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
