histex pd drops new formulation

Generic: triprolidine hydrochloride

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

Drug Facts

Product Profile

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

triprolidine hydrochloride 1.25 mg/mL

Manufacturer
Allegis Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 28595-809
Product ID 28595-809_2b39e554-da95-1979-e063-6394a90a887a
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2023-12-13

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 28595809
Hyphenated Format 28595-809

Supplemental Identifiers

RxCUI
1926926
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 pd drops new formulation (source: ndc)
Generic Name triprolidine hydrochloride (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1.25 mg/mL
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (28595-809-30) / 30 mL in 1 BOTTLE
source: ndc

Packages (1)

Ingredients (1)

triprolidine hydrochloride (1.25 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2b39e554-da95-1979-e063-6394a90a887a", "openfda": {"unii": ["YAN7R5L890"], "rxcui": ["1926926"], "spl_set_id": ["0c693f15-5d76-3dbf-e063-6294a90af9ac"], "manufacturer_name": ["Allegis Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (28595-809-30)  / 30 mL in 1 BOTTLE", "package_ndc": "28595-809-30", "marketing_start_date": "20231213"}], "brand_name": "HISTEX PD Drops New Formulation", "product_id": "28595-809_2b39e554-da95-1979-e063-6394a90a887a", "dosage_form": "SYRUP", "product_ndc": "28595-809", "generic_name": "TRIPROLIDINE HYDROCHLORIDE", "labeler_name": "Allegis Pharmaceuticals, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "HISTEX PD Drops New Formulation", "active_ingredients": [{"name": "TRIPROLIDINE HYDROCHLORIDE", "strength": "1.25 mg/mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20231213", "listing_expiration_date": "20261231"}