diphenhydramine
Generic: diphenhydramine hydrochloride
Labeler: micro labs limitedDrug Facts
Product Profile
Brand Name
diphenhydramine
Generic Name
diphenhydramine hydrochloride
Labeler
micro labs limited
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
diphenhydramine hydrochloride 50 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
42571-169
Product ID
42571-169_4c46492b-00c4-8ee4-e063-6294a90a6914
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA205723
Listing Expiration
2027-12-31
Marketing Start
2018-12-04
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
42571169
Hyphenated Format
42571-169
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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 (source: ndc)
Generic Name
diphenhydramine hydrochloride (source: ndc)
Application Number
ANDA205723 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/mL
Packaging
- 10 AMPULE in 1 CARTON (42571-169-55) / 1 mL in 1 AMPULE (42571-169-54)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "4c46492b-00c4-8ee4-e063-6294a90a6914", "openfda": {"upc": ["0342571337957", "0342571169541"], "unii": ["TC2D6JAD40"], "rxcui": ["1723740"], "spl_set_id": ["a1110433-498a-48cb-ac79-5732fd4f8fba"], "manufacturer_name": ["Micro Labs Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 AMPULE in 1 CARTON (42571-169-55) / 1 mL in 1 AMPULE (42571-169-54)", "package_ndc": "42571-169-55", "marketing_start_date": "20181204"}], "brand_name": "DIPHENHYDRAMINE", "product_id": "42571-169_4c46492b-00c4-8ee4-e063-6294a90a6914", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "42571-169", "generic_name": "Diphenhydramine Hydrochloride", "labeler_name": "Micro Labs Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DIPHENHYDRAMINE", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "50 mg/mL"}], "application_number": "ANDA205723", "marketing_category": "ANDA", "marketing_start_date": "20181204", "listing_expiration_date": "20271231"}