Auvi-Q (Page 5 of 5)

PRINCIPAL DISPLAY PANEL — Outer Package Label

71872-7173-1 PDP
(click image for full-size original)

PRINCIPAL DISPLAY PANEL — 0.3 mg Case Label

0.3 mg Outer Case Label
(click image for full-size original)

PRINCIPAL DISPLAY PANEL — 0.3 mg Device Label

0.3 mg Device Label
(click image for full-size original)

AUVI-Q epinephrine injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:71872-7173(NDC:60842-023)
Route of Administration INTRAMUSCULAR DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
EPINEPHRINE (EPINEPHRINE) EPINEPHRINE 0.3 mg in 0.3 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE 2.3 mg in 0.3 mL
SODIUM BISULFITE 0.5 mg in 0.3 mL
WATER
HYDROCHLORIC ACID
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:71872-7173-1 1 DOSE PACK in 1 BAG contains a DOSE PACK
1 0.3 mL in 1 DOSE PACK This package is contained within the BAG (71872-7173-1)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA201739 11/15/2012
Labeler — Medical Purchasing Solutions, LLC (601458529)
Establishment
Name Address ID/FEI Operations
Medical Purchasing Solutions, LLC 601458529 repack (71872-7173)

Revised: 08/2019 Medical Purchasing Solutions, LLC

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