diphenhydramine hydrochloride
Generic: diphenhydramine hydrochloride
Labeler: major pharmaceuticalsDrug Facts
Product Profile
Brand Name
diphenhydramine hydrochloride
Generic Name
diphenhydramine hydrochloride
Labeler
major pharmaceuticals
Dosage Form
CAPSULE
Routes
Active Ingredients
diphenhydramine hydrochloride 50 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0904-2056
Product ID
0904-2056_4b432cbb-d3d9-2f88-e063-6294a90a7ed5
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Marketing Start
2009-01-02
Marketing End
2027-12-31
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
09042056
Hyphenated Format
0904-2056
Supplemental Identifiers
RxCUI
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
M012 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/1
Packaging
- 10 BLISTER PACK in 1 BOX (0904-2056-61) / 10 CAPSULE in 1 BLISTER PACK
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4b432cbb-d3d9-2f88-e063-6294a90a7ed5", "openfda": {"unii": ["TC2D6JAD40"], "rxcui": ["1020477", "1049909", "1092422"], "spl_set_id": ["04e70311-6412-4a20-84e3-f6e26d5f19ab"], "manufacturer_name": ["Major Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 BOX (0904-2056-61) / 10 CAPSULE in 1 BLISTER PACK", "package_ndc": "0904-2056-61", "marketing_end_date": "20271231", "marketing_start_date": "20090102"}], "brand_name": "Diphenhydramine Hydrochloride", "product_id": "0904-2056_4b432cbb-d3d9-2f88-e063-6294a90a7ed5", "dosage_form": "CAPSULE", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "0904-2056", "generic_name": "Diphenhydramine Hydrochloride", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Diphenhydramine Hydrochloride", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20271231", "marketing_start_date": "20090102"}