dicyclomine hydrochloride

Generic: dicyclomine hydrochloride

Labeler: solaris pharma corporation
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name dicyclomine hydrochloride
Generic Name dicyclomine hydrochloride
Labeler solaris pharma corporation
Dosage Form TABLET
Routes
ORAL
Active Ingredients

dicyclomine hydrochloride 20 mg/1

Manufacturer
Solaris Pharma Corporation

Identifiers & Regulatory

Product NDC 73473-902
Product ID 73473-902_98b3a053-2708-460d-9929-d89164cd4a49
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216760
Listing Expiration 2026-12-31
Marketing Start 2025-06-10

Pharmacologic Class

Classes
anticholinergic [epc] cholinergic antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 73473902
Hyphenated Format 73473-902

Supplemental Identifiers

RxCUI
991086
UPC
0373473902103 0373473902011
UNII
CQ903KQA31

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 dicyclomine hydrochloride (source: ndc)
Generic Name dicyclomine hydrochloride (source: ndc)
Application Number ANDA216760 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (73473-902-01)
  • 1000 TABLET in 1 BOTTLE (73473-902-10)
source: ndc

Packages (2)

73473-902-01 100 TABLET in 1 BOTTLE (73473-902-01) 73473-902-10 1000 TABLET in 1 BOTTLE (73473-902-10)

Ingredients (1)

dicyclomine hydrochloride (20 mg/1)

Linked Drug Pages (1)

DICYCLOMINE HYDROCHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "98b3a053-2708-460d-9929-d89164cd4a49", "openfda": {"upc": ["0373473902103", "0373473902011"], "unii": ["CQ903KQA31"], "rxcui": ["991086"], "spl_set_id": ["d46259e6-5eca-4356-bc18-815104c925cc"], "manufacturer_name": ["Solaris Pharma Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (73473-902-01)", "package_ndc": "73473-902-01", "marketing_start_date": "20250610"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (73473-902-10)", "package_ndc": "73473-902-10", "marketing_start_date": "20250610"}], "brand_name": "DICYCLOMINE HYDROCHLORIDE", "product_id": "73473-902_98b3a053-2708-460d-9929-d89164cd4a49", "dosage_form": "TABLET", "pharm_class": ["Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]"], "product_ndc": "73473-902", "generic_name": "DICYCLOMINE HYDROCHLORIDE", "labeler_name": "Solaris Pharma Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DICYCLOMINE HYDROCHLORIDE", "active_ingredients": [{"name": "DICYCLOMINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA216760", "marketing_category": "ANDA", "marketing_start_date": "20250610", "listing_expiration_date": "20261231"}