triprolidine hydrochloride

Generic: triprolidine hydrochloride

Labeler: westminster pharmaceuticals, llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name triprolidine hydrochloride
Generic Name triprolidine hydrochloride
Labeler westminster pharmaceuticals, llc
Dosage Form SYRUP
Routes
ORAL
Active Ingredients

triprolidine hydrochloride .938 mg/mL

Manufacturer
Westminster Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 69367-253
Product ID 69367-253_63d97fa4-9b2d-4eef-8865-0cc4af5bc9e8
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2020-03-09

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69367253
Hyphenated Format 69367-253

Supplemental Identifiers

RxCUI
1491649
UPC
0369367253307
UNII
YAN7R5L890

Packaging Origin

Original Packager
true

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 triprolidine hydrochloride (source: ndc)
Generic Name triprolidine hydrochloride (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .938 mg/mL
source: ndc
Packaging
  • 1 BOTTLE, DROPPER in 1 CARTON (69367-253-30) / 30 mL in 1 BOTTLE, DROPPER
source: ndc

Packages (1)

69367-253-30 1 BOTTLE, DROPPER in 1 CARTON (69367-253-30) / 30 mL in 1 BOTTLE, DROPPER

Ingredients (1)

triprolidine hydrochloride (.938 mg/mL)

Linked Drug Pages (1)

TRIPROLIDINE HYDROCHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "63d97fa4-9b2d-4eef-8865-0cc4af5bc9e8", "openfda": {"upc": ["0369367253307"], "unii": ["YAN7R5L890"], "rxcui": ["1491649"], "spl_set_id": ["a9f01760-e335-4410-a9b8-8edce2841270"], "manufacturer_name": ["Westminster Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, DROPPER in 1 CARTON (69367-253-30)  / 30 mL in 1 BOTTLE, DROPPER", "package_ndc": "69367-253-30", "marketing_start_date": "20200309"}], "brand_name": "TRIPROLIDINE HYDROCHLORIDE", "product_id": "69367-253_63d97fa4-9b2d-4eef-8865-0cc4af5bc9e8", "dosage_form": "SYRUP", "product_ndc": "69367-253", "generic_name": "TRIPROLIDINE HYDROCHLORIDE", "labeler_name": "Westminster Pharmaceuticals, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "TRIPROLIDINE HYDROCHLORIDE", "active_ingredients": [{"name": "TRIPROLIDINE HYDROCHLORIDE", "strength": ".938 mg/mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200309", "listing_expiration_date": "20261231"}