diphenhydramine hydrochloride
Generic: diphenhydramine hydrochloride
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
diphenhydramine hydrochloride
Generic Name
diphenhydramine hydrochloride
Labeler
remedyrepack inc.
Dosage Form
INJECTION
Routes
Active Ingredients
diphenhydramine hydrochloride 50 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
70518-1082
Product ID
70518-1082_485992c3-e3e0-e79a-e063-6294a90a655b
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA080817
Listing Expiration
2027-12-31
Marketing Start
2018-03-27
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705181082
Hyphenated Format
70518-1082
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
ANDA080817 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/mL
Packaging
- 25 VIAL in 1 PACKAGE (70518-1082-1) / 1 mL in 1 VIAL (70518-1082-0)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "485992c3-e3e0-e79a-e063-6294a90a655b", "openfda": {"unii": ["TC2D6JAD40"], "rxcui": ["1049633"], "spl_set_id": ["62edde3d-b41b-40fc-ac18-b749035de831"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 PACKAGE (70518-1082-1) / 1 mL in 1 VIAL (70518-1082-0)", "package_ndc": "70518-1082-1", "marketing_start_date": "20180327"}], "brand_name": "Diphenhydramine Hydrochloride", "product_id": "70518-1082_485992c3-e3e0-e79a-e063-6294a90a655b", "dosage_form": "INJECTION", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "70518-1082", "generic_name": "diphenhydramine hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diphenhydramine Hydrochloride", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "50 mg/mL"}], "application_number": "ANDA080817", "marketing_category": "ANDA", "marketing_start_date": "20180327", "listing_expiration_date": "20271231"}