HISTEX PD Drops
Generic: TRIPROLIDINE HYDROCHLORIDE
Labeler: Allegis Pharmaceuticals, LLCDrug Facts
Product Profile
Brand Name
HISTEX PD Drops
Generic Name
TRIPROLIDINE HYDROCHLORIDE
Labeler
Allegis Pharmaceuticals, LLC
Dosage Form
SYRUP
Routes
Active Ingredients
TRIPROLIDINE HYDROCHLORIDE .938 mg/mL
Identifiers & Regulatory
Product NDC
28595-801
Product ID
28595-801_0e7690d0-b1d3-bc5e-e063-6294a90afc18
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Listing Expiration
2026-12-31
Marketing Start
2014-03-06
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
28595801
Hyphenated Format
28595-801
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 (source: ndc)
Generic Name
TRIPROLIDINE HYDROCHLORIDE (source: ndc)
Application Number
M012 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .938 mg/mL
Packaging
- 1 BOTTLE in 1 CARTON (28595-801-30) / 30 mL in 1 BOTTLE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0e7690d0-b1d3-bc5e-e063-6294a90afc18", "openfda": {"unii": ["YAN7R5L890"], "rxcui": ["1491649"], "spl_set_id": ["0a55c379-ac91-461f-bdbe-1a4af39d68d4"], "manufacturer_name": ["Allegis Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (28595-801-30) / 30 mL in 1 BOTTLE", "package_ndc": "28595-801-30", "marketing_start_date": "20140306"}], "brand_name": "HISTEX PD Drops", "product_id": "28595-801_0e7690d0-b1d3-bc5e-e063-6294a90afc18", "dosage_form": "SYRUP", "product_ndc": "28595-801", "generic_name": "TRIPROLIDINE HYDROCHLORIDE", "labeler_name": "Allegis Pharmaceuticals, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "HISTEX PD Drops", "active_ingredients": [{"name": "TRIPROLIDINE HYDROCHLORIDE", "strength": ".938 mg/mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20140306", "listing_expiration_date": "20261231"}