dicyclomine hydrochloride
Generic: dicyclomine hydrochloride
Labeler: endo usa, inc.Drug Facts
Product Profile
Brand Name
dicyclomine hydrochloride
Generic Name
dicyclomine hydrochloride
Labeler
endo usa, inc.
Dosage Form
SOLUTION
Routes
Active Ingredients
dicyclomine hydrochloride 10 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
0603-1161
Product ID
0603-1161_5f04cd24-b303-43dc-a963-f28d35a275ff
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA040169
Listing Expiration
2026-12-31
Marketing Start
2005-06-23
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
06031161
Hyphenated Format
0603-1161
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
ANDA040169 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/5mL
Packaging
- 473 mL in 1 BOTTLE, PLASTIC (0603-1161-58)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "5f04cd24-b303-43dc-a963-f28d35a275ff", "openfda": {"unii": ["CQ903KQA31"], "rxcui": ["991082"], "spl_set_id": ["bb099db9-f635-4a64-8892-6236971dec45"], "manufacturer_name": ["Endo USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE, PLASTIC (0603-1161-58)", "package_ndc": "0603-1161-58", "marketing_start_date": "20050623"}], "brand_name": "dicyclomine hydrochloride", "product_id": "0603-1161_5f04cd24-b303-43dc-a963-f28d35a275ff", "dosage_form": "SOLUTION", "pharm_class": ["Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]"], "product_ndc": "0603-1161", "generic_name": "dicyclomine hydrochloride", "labeler_name": "Endo USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "dicyclomine hydrochloride", "active_ingredients": [{"name": "DICYCLOMINE HYDROCHLORIDE", "strength": "10 mg/5mL"}], "application_number": "ANDA040169", "marketing_category": "ANDA", "marketing_start_date": "20050623", "listing_expiration_date": "20261231"}