trospium chloride
Generic: trospium chloride
Labeler: pd-rx pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
trospium chloride
Generic Name
trospium chloride
Labeler
pd-rx pharmaceuticals, inc.
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
trospium chloride 20 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72789-348
Product ID
72789-348_40bb63a7-468a-a247-e063-6394a90acced
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA091573
Listing Expiration
2026-12-31
Marketing Start
2010-11-17
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72789348
Hyphenated Format
72789-348
Supplemental Identifiers
RxCUI
UPC
UNII
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
trospium chloride (source: ndc)
Generic Name
trospium chloride (source: ndc)
Application Number
ANDA091573 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/1
Packaging
- 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-348-60)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "40bb63a7-468a-a247-e063-6394a90acced", "openfda": {"upc": ["0372789348605"], "unii": ["1E6682427E"], "rxcui": ["857560"], "spl_set_id": ["6303cf3c-175c-46ff-9b88-05f6ea7a2135"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-348-60)", "package_ndc": "72789-348-60", "marketing_start_date": "20230829"}], "brand_name": "TROSPIUM CHLORIDE", "product_id": "72789-348_40bb63a7-468a-a247-e063-6394a90acced", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "72789-348", "generic_name": "TROSPIUM CHLORIDE", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "TROSPIUM CHLORIDE", "active_ingredients": [{"name": "TROSPIUM CHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA091573", "marketing_category": "ANDA", "marketing_start_date": "20101117", "listing_expiration_date": "20261231"}