diphenhydramine hydrochloride
Generic: diphenhydramine hydrochloride
Labeler: propharma distributionDrug Facts
Product Profile
Brand Name
diphenhydramine hydrochloride
Generic Name
diphenhydramine hydrochloride
Labeler
propharma distribution
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
diphenhydramine hydrochloride 50 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
84549-101
Product ID
84549-101_463c9f3f-5718-c3fc-e063-6294a90a60aa
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA205723
Listing Expiration
2026-12-31
Marketing Start
2019-05-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
84549101
Hyphenated Format
84549-101
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
ANDA205723 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/mL
Packaging
- 1 mL in 1 VIAL, SINGLE-DOSE (84549-101-25)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "463c9f3f-5718-c3fc-e063-6294a90a60aa", "openfda": {"unii": ["TC2D6JAD40"], "rxcui": ["1723740"], "spl_set_id": ["3842d802-9b18-2c5e-e063-6394a90ae763"], "manufacturer_name": ["ProPharma Distribution"]}, "finished": true, "packaging": [{"sample": false, "description": "1 mL in 1 VIAL, SINGLE-DOSE (84549-101-25)", "package_ndc": "84549-101-25", "marketing_start_date": "20250827"}], "brand_name": "Diphenhydramine Hydrochloride", "product_id": "84549-101_463c9f3f-5718-c3fc-e063-6294a90a60aa", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "84549-101", "generic_name": "Diphenhydramine Hydrochloride", "labeler_name": "ProPharma Distribution", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diphenhydramine Hydrochloride", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "50 mg/mL"}], "application_number": "ANDA205723", "marketing_category": "ANDA", "marketing_start_date": "20190501", "listing_expiration_date": "20261231"}