Diphenhydramine hydrochloride

Product NDC
70518-4455
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
diphenhydramine hydrochloride
Dosage form
INJECTION
Route
INTRAMUSCULAR; INTRAVENOUS
Labeler
REMEDYREPACK INC.
Application
ANDA080817
Marketing category
ANDA
Substance
DIPHENHYDRAMINE HYDROCHLORIDE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
70518-4455-025 VIAL in 1 PACKAGE (70518-4455-0) / 1 mL in 1 VIAL (70518-4455-1) 2025-08-23NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Diphenhydramine Hydrochloride Injection, USP Rx onlyREMEDYREPACK INC.2025-08-25HUMAN PRESCRIPTION DRUG LABEL1