histex

Generic: triprolidine hydrochloride

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

Drug Facts

Product Profile

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

triprolidine hydrochloride 2.5 mg/5mL

Manufacturer
Allegis Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 28595-802
Product ID 28595-802_0e764061-e7a9-6701-e063-6394a90a489f
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2014-03-04

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 28595802
Hyphenated Format 28595-802

Supplemental Identifiers

RxCUI
1490671
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 histex (source: ndc)
Generic Name triprolidine hydrochloride (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2.5 mg/5mL
source: ndc
Packaging
  • 237 mL in 1 BOTTLE (28595-802-08)
source: ndc

Packages (1)

28595-802-08 237 mL in 1 BOTTLE (28595-802-08)

Ingredients (1)

triprolidine hydrochloride (2.5 mg/5mL)

Linked Drug Pages (1)

HISTEX ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0e764061-e7a9-6701-e063-6394a90a489f", "openfda": {"unii": ["YAN7R5L890"], "rxcui": ["1490671"], "spl_set_id": ["cc466d33-cf3e-4f1c-a794-6d3d79903adf"], "manufacturer_name": ["Allegis Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "237 mL in 1 BOTTLE (28595-802-08)", "package_ndc": "28595-802-08", "marketing_start_date": "20140304"}], "brand_name": "HISTEX", "product_id": "28595-802_0e764061-e7a9-6701-e063-6394a90a489f", "dosage_form": "SYRUP", "product_ndc": "28595-802", "generic_name": "TRIPROLIDINE HYDROCHLORIDE", "labeler_name": "Allegis Pharmaceuticals, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "HISTEX", "active_ingredients": [{"name": "TRIPROLIDINE HYDROCHLORIDE", "strength": "2.5 mg/5mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20140304", "listing_expiration_date": "20261231"}