dicyclomine hydrochloride
Generic: dicyclomine hydrochloride
Labeler: pd-rx pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
dicyclomine hydrochloride
Generic Name
dicyclomine hydrochloride
Labeler
pd-rx pharmaceuticals, inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
dicyclomine hydrochloride 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
43063-112
Product ID
43063-112_2b251781-1d01-12a3-e063-6394a90a1963
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA085082
Listing Expiration
2026-12-31
Marketing Start
1986-06-19
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
43063112
Hyphenated Format
43063-112
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
ANDA085082 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 4 CAPSULE in 1 BOTTLE, PLASTIC (43063-112-04)
- 6 CAPSULE in 1 BOTTLE, PLASTIC (43063-112-06)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2b251781-1d01-12a3-e063-6394a90a1963", "openfda": {"unii": ["CQ903KQA31"], "rxcui": ["991061"], "spl_set_id": ["8c29140b-e181-4807-870f-28e315c6d4c4"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "4 CAPSULE in 1 BOTTLE, PLASTIC (43063-112-04)", "package_ndc": "43063-112-04", "marketing_start_date": "20110307"}, {"sample": false, "description": "6 CAPSULE in 1 BOTTLE, PLASTIC (43063-112-06)", "package_ndc": "43063-112-06", "marketing_start_date": "20110307"}], "brand_name": "Dicyclomine Hydrochloride", "product_id": "43063-112_2b251781-1d01-12a3-e063-6394a90a1963", "dosage_form": "CAPSULE", "pharm_class": ["Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]"], "product_ndc": "43063-112", "generic_name": "Dicyclomine Hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dicyclomine Hydrochloride", "active_ingredients": [{"name": "DICYCLOMINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA085082", "marketing_category": "ANDA", "marketing_start_date": "19860619", "listing_expiration_date": "20261231"}