allergy
Generic: diphenhydramine hydrochloride
Labeler: velocity pharma llcDrug Facts
Product Profile
Brand Name
allergy
Generic Name
diphenhydramine hydrochloride
Labeler
velocity pharma llc
Dosage Form
TABLET
Routes
Active Ingredients
diphenhydramine hydrochloride 25 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
76168-121
Product ID
76168-121_6c30ec6a-4c24-d604-e053-2a91aa0ac869
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH FINAL
Application Number
part341
Listing Expiration
2026-12-31
Marketing Start
2018-05-14
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
76168121
Hyphenated Format
76168-121
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
allergy (source: ndc)
Generic Name
diphenhydramine hydrochloride (source: ndc)
Application Number
part341 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 mg/1
Packaging
- 100 CARTON in 1 BOTTLE (76168-121-12) / 1 TABLET in 1 CARTON
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6c30ec6a-4c24-d604-e053-2a91aa0ac869", "openfda": {"unii": ["TC2D6JAD40"], "rxcui": ["1049630"], "spl_set_id": ["73e4f21c-e5ec-42c9-9ec8-118479857057"], "manufacturer_name": ["Velocity Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CARTON in 1 BOTTLE (76168-121-12) / 1 TABLET in 1 CARTON", "package_ndc": "76168-121-12", "marketing_start_date": "20180514"}], "brand_name": "Allergy", "product_id": "76168-121_6c30ec6a-4c24-d604-e053-2a91aa0ac869", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "76168-121", "generic_name": "Diphenhydramine Hydrochloride", "labeler_name": "Velocity Pharma LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Allergy", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "part341", "marketing_category": "OTC MONOGRAPH FINAL", "marketing_start_date": "20180514", "listing_expiration_date": "20261231"}