dicyclomine hydrochloride
Generic: dicyclomine hydrochloride
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
dicyclomine hydrochloride
Generic Name
dicyclomine hydrochloride
Labeler
remedyrepack inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
dicyclomine hydrochloride 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70518-4331
Product ID
70518-4331_40301a39-d985-9366-e063-6394a90acdd9
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA040319
Listing Expiration
2026-12-31
Marketing Start
2025-04-19
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705184331
Hyphenated Format
70518-4331
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
dicyclomine hydrochloride (source: ndc)
Generic Name
dicyclomine hydrochloride (source: ndc)
Application Number
ANDA040319 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 30 CAPSULE in 1 BLISTER PACK (70518-4331-0)
- 30 CAPSULE in 1 BOTTLE, PLASTIC (70518-4331-1)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "40301a39-d985-9366-e063-6394a90acdd9", "openfda": {"unii": ["CQ903KQA31"], "rxcui": ["991061"], "spl_set_id": ["e67ad329-6395-4fa0-a898-f13959034e26"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (70518-4331-0)", "package_ndc": "70518-4331-0", "marketing_start_date": "20250419"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE, PLASTIC (70518-4331-1)", "package_ndc": "70518-4331-1", "marketing_start_date": "20250827"}], "brand_name": "Dicyclomine Hydrochloride", "product_id": "70518-4331_40301a39-d985-9366-e063-6394a90acdd9", "dosage_form": "CAPSULE", "pharm_class": ["Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]"], "product_ndc": "70518-4331", "generic_name": "Dicyclomine Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dicyclomine Hydrochloride", "active_ingredients": [{"name": "DICYCLOMINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA040319", "marketing_category": "ANDA", "marketing_start_date": "20250419", "listing_expiration_date": "20261231"}