diphenhydramine hydrochloride
Generic: diphenhydramine hydrochloride
Labeler: hf acquisition co llc, dba healthfirstDrug Facts
Product Profile
Brand Name
diphenhydramine hydrochloride
Generic Name
diphenhydramine hydrochloride
Labeler
hf acquisition co llc, dba healthfirst
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
diphenhydramine hydrochloride 50 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
51662-1348
Product ID
51662-1348_ef7bd6e6-d62c-7e93-e053-2a95a90aef83
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA040466
Listing Expiration
2026-12-31
Marketing Start
2018-11-26
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
516621348
Hyphenated Format
51662-1348
Supplemental Identifiers
RxCUI
UNII
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
diphenhydramine hydrochloride (source: ndc)
Generic Name
diphenhydramine hydrochloride (source: ndc)
Application Number
ANDA040466 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/mL
Packaging
- 1 mL in 1 VIAL (51662-1348-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "ef7bd6e6-d62c-7e93-e053-2a95a90aef83", "openfda": {"unii": ["TC2D6JAD40"], "rxcui": ["1723740"], "spl_set_id": ["7b9ed8ef-ce21-19e7-e053-2a91aa0a81be"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "1 mL in 1 VIAL (51662-1348-1)", "package_ndc": "51662-1348-1", "marketing_start_date": "20181126"}], "brand_name": "DIPHENHYDRAMINE HYDROCHLORIDE", "product_id": "51662-1348_ef7bd6e6-d62c-7e93-e053-2a95a90aef83", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "51662-1348", "generic_name": "DIPHENHYDRAMINE HYDROCHLORIDE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DIPHENHYDRAMINE HYDROCHLORIDE", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "50 mg/mL"}], "application_number": "ANDA040466", "marketing_category": "ANDA", "marketing_start_date": "20181126", "listing_expiration_date": "20261231"}