NDC Code(s) : 49349-836-01
Packager : REMEDYREPACK INC.

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

Diphenhydramine Hydrochloride diphenhydramine hydrochloride INJECTION
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:49349-836(NDC:0641-0376)
Route of Administration INTRAMUSCULAR DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
DIPHENHYDRAMINE HYDROCHLORIDE(UNII: TC2D6JAD40)
(DIPHENHYDRAMINE - UNII:8GTS82S83M) 		DIPHENHYDRAMINE HYDROCHLORIDE50 mg in 1 mL
Inactive Ingredients
Ingredient Name Strength
BENZETHONIUM CHLORIDE(UNII: PH41D05744)
SODIUM HYDROXIDE(UNII: 55X04QC32I)
HYDROCHLORIC ACID(UNII: QTT17582CB)
WATER(UNII: 059QF0KO0R)
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:49349-836-011 mL in 1 VIAL Type 0: Not a Combination Product
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA080817 07/24/2015

PRINCIPAL DISPLAY PANEL

DRUG: Diphenhydramine Hydrochloride


GENERIC: diphenhydramine hydrochloride


DOSAGE: INJECTION


ADMINSTRATION: INTRAMUSCULAR


NDC: 49349-836-01


ACTIVE INGREDIENT(S):

  • DIPHENHYDRAMINE HYDROCHLORIDE 50mg in 1mL


INACTIVE INGREDIENT(S):

  • BENZETHONIUM CHLORIDE
  • SODIUM HYDROXIDE
  • HYDROCHLORIC ACID
  • WATER


PACKAGING: 1 mL in 1 VIAL




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