diphenhydramine hydrochloride
Generic: diphenhydramine hydrochloride
Labeler: aaa pharmaceutical, inc.Drug Facts
Product Profile
Brand Name
diphenhydramine hydrochloride
Generic Name
diphenhydramine hydrochloride
Labeler
aaa pharmaceutical, inc.
Dosage Form
TABLET, COATED
Routes
Active Ingredients
diphenhydramine hydrochloride 25 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
57344-091
Product ID
57344-091_284d2782-2253-c0b9-e063-6394a90aaeb3
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M010
Listing Expiration
2026-12-31
Marketing Start
2018-10-05
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
57344091
Hyphenated Format
57344-091
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 hydrochloride (source: ndc)
Generic Name
diphenhydramine hydrochloride (source: ndc)
Application Number
M010 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 mg/1
Packaging
- 1 BOTTLE, PLASTIC in 1 CARTON (57344-091-03) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "284d2782-2253-c0b9-e063-6394a90aaeb3", "openfda": {"upc": ["0099581911737"], "unii": ["TC2D6JAD40"], "rxcui": ["1049630"], "spl_set_id": ["c280cf02-ebb2-4847-a66d-d02aff3ea0c9"], "manufacturer_name": ["AAA Pharmaceutical, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (57344-091-03) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "57344-091-03", "marketing_start_date": "20181005"}], "brand_name": "Diphenhydramine Hydrochloride", "product_id": "57344-091_284d2782-2253-c0b9-e063-6394a90aaeb3", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "57344-091", "generic_name": "DIPHENHYDRAMINE HYDROCHLORIDE", "labeler_name": "AAA Pharmaceutical, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Diphenhydramine Hydrochloride", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M010", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20181005", "listing_expiration_date": "20261231"}