trospium chloride
Generic: trospium chloride
Labeler: major pharmaceuticalsDrug Facts
Product Profile
Brand Name
trospium chloride
Generic Name
trospium chloride
Labeler
major pharmaceuticals
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
trospium chloride 20 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0904-7059
Product ID
0904-7059_239e206f-f6ca-4b35-a5b0-46d255cd57fa
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA204945
Listing Expiration
2026-12-31
Marketing Start
2015-11-16
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
09047059
Hyphenated Format
0904-7059
Supplemental Identifiers
RxCUI
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
ANDA204945 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/1
Packaging
- 60 TABLET, FILM COATED in 1 BOTTLE (0904-7059-52)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "239e206f-f6ca-4b35-a5b0-46d255cd57fa", "openfda": {"unii": ["1E6682427E"], "rxcui": ["857560"], "spl_set_id": ["35ae4d64-4625-4fdd-a2d4-e20b87c56876"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (0904-7059-52)", "package_ndc": "0904-7059-52", "marketing_start_date": "20151116"}], "brand_name": "Trospium Chloride", "product_id": "0904-7059_239e206f-f6ca-4b35-a5b0-46d255cd57fa", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "0904-7059", "generic_name": "Trospium Chloride", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trospium Chloride", "active_ingredients": [{"name": "TROSPIUM CHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA204945", "marketing_category": "ANDA", "marketing_start_date": "20151116", "listing_expiration_date": "20261231"}