dicyclomine hydrochloride
Generic: dicyclomine hydrochloride
Labeler: american health packagingDrug Facts
Product Profile
Brand Name
dicyclomine hydrochloride
Generic Name
dicyclomine hydrochloride
Labeler
american health packaging
Dosage Form
TABLET
Routes
Active Ingredients
dicyclomine hydrochloride 20 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
60687-380
Product ID
60687-380_20d5c3bc-5e5b-8cfe-e063-6394a90a5618
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA040230
Listing Expiration
2026-12-31
Marketing Start
2018-12-06
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
60687380
Hyphenated Format
60687-380
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
ANDA040230 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/1
Packaging
- 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-380-01) / 1 TABLET in 1 BLISTER PACK (60687-380-11)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "20d5c3bc-5e5b-8cfe-e063-6394a90a5618", "openfda": {"unii": ["CQ903KQA31"], "rxcui": ["991061", "991086"], "spl_set_id": ["833c5d7c-85ca-4ce3-bcd8-5e5b4ecbffe8"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-380-01) / 1 TABLET in 1 BLISTER PACK (60687-380-11)", "package_ndc": "60687-380-01", "marketing_start_date": "20181206"}], "brand_name": "Dicyclomine Hydrochloride", "product_id": "60687-380_20d5c3bc-5e5b-8cfe-e063-6394a90a5618", "dosage_form": "TABLET", "pharm_class": ["Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]"], "product_ndc": "60687-380", "generic_name": "Dicyclomine Hydrochloride", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dicyclomine Hydrochloride", "active_ingredients": [{"name": "DICYCLOMINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA040230", "marketing_category": "ANDA", "marketing_start_date": "20181206", "listing_expiration_date": "20261231"}