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GlucaGen
GlucaGen - 55390-004-01 - (glucagon hydrochloride)
Drug Information of GlucaGen
| Product NDC: | 55390-004 |
| Proprietary Name: | GlucaGen |
| Non Proprietary Name: | glucagon hydrochloride |
| Active Ingredient(s): | & nbsp; glucagon hydrochloride |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of GlucaGen
| Product NDC: | 55390-004 |
| Labeler Name: | Bedford Laboratories |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020918 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20050622 |
Package Information of GlucaGen
| Package NDC: | 55390-004-01 |
| Package Description: | 1 KIT in 1 KIT (55390-004-01) * 10 VIAL, GLASS in 1 CARTON > 1 mL in 1 VIAL, GLASS * 1 mL in 1 VIAL, GLASS |
NDC Information of GlucaGen
| NDC Code | 55390-004-01 |
| Proprietary Name | GlucaGen |
| Package Description | 1 KIT in 1 KIT (55390-004-01) * 10 VIAL, GLASS in 1 CARTON > 1 mL in 1 VIAL, GLASS * 1 mL in 1 VIAL, GLASS |
| Product NDC | 55390-004 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | glucagon hydrochloride |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20050622 |
| Marketing Category Name | NDA |
| Labeler Name | Bedford Laboratories |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
