NDC 0002-7529 - GLUCAG0N

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
0002-7529
Package NDCs from labels
0002-7529-01
Manufacturer
HF Acquisition Co LLC, DBA HealthFirst
Effective date
2022-12-09
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
GLUCAG0N - HF Acquisition Co LLC, DBA HealthFirstHF Acquisition Co LLC, DBA HealthFirst2022-12-09HUMAN PRESCRIPTION DRUG LABEL
Diluting Solution for Glucagon - TYA PharmaceuticalsTYA Pharmaceuticals2013-10-03HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0002-7529-01Glucagon1 mL in 1 VIALINJECTION, POWDER, FOR SOLUTION1 mL1 mg in 1mL2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0002-7529GLUCAGON KIT [TYA PHARMACEUTICALS]2Unmatched20140930_b53a7c5d-2de6-40a3-9015-ca18cf84df19.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
glucagonACTIVE INGREDIENT76LA80IG2GGLUCAGON KIT [TYA PHARMACEUTICALS]2
glucagonACTIVE MOIETY76LA80IG2GGLUCAGON KIT [TYA PHARMACEUTICALS]2
HYDROCHLORIC ACIDINACTIVE INGREDIENTQTT17582CBGLUCAGON KIT [TYA PHARMACEUTICALS]2
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GGLUCAGON KIT [TYA PHARMACEUTICALS]2