dicyclomine hydrochloride

Generic: dicyclomine hydrochloride

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name dicyclomine hydrochloride
Generic Name dicyclomine hydrochloride
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

dicyclomine hydrochloride 20 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 63187-784
Product ID 63187-784_2bab7712-de3d-45a1-a21c-b6273721bb28
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA085223
Listing Expiration 2026-12-31
Marketing Start 1986-07-30

Pharmacologic Class

Classes
anticholinergic [epc] cholinergic antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63187784
Hyphenated Format 63187-784

Supplemental Identifiers

RxCUI
991086
UPC
0363187784157
UNII
CQ903KQA31

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 ANDA085223 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 15 TABLET in 1 BOTTLE, PLASTIC (63187-784-15)
  • 20 TABLET in 1 BOTTLE, PLASTIC (63187-784-20)
  • 30 TABLET in 1 BOTTLE, PLASTIC (63187-784-30)
  • 60 TABLET in 1 BOTTLE, PLASTIC (63187-784-60)
  • 90 TABLET in 1 BOTTLE, PLASTIC (63187-784-90)
source: ndc

Packages (5)

63187-784-15 15 TABLET in 1 BOTTLE, PLASTIC (63187-784-15) 63187-784-20 20 TABLET in 1 BOTTLE, PLASTIC (63187-784-20) 63187-784-30 30 TABLET in 1 BOTTLE, PLASTIC (63187-784-30) 63187-784-60 60 TABLET in 1 BOTTLE, PLASTIC (63187-784-60) 63187-784-90 90 TABLET in 1 BOTTLE, PLASTIC (63187-784-90)

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": "2bab7712-de3d-45a1-a21c-b6273721bb28", "openfda": {"upc": ["0363187784157"], "unii": ["CQ903KQA31"], "rxcui": ["991086"], "spl_set_id": ["bd8b7fcd-04f4-4d1c-aa27-743aaf4c2876"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET in 1 BOTTLE, PLASTIC (63187-784-15)", "package_ndc": "63187-784-15", "marketing_start_date": "20161101"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE, PLASTIC (63187-784-20)", "package_ndc": "63187-784-20", "marketing_start_date": "20161101"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (63187-784-30)", "package_ndc": "63187-784-30", "marketing_start_date": "20161101"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (63187-784-60)", "package_ndc": "63187-784-60", "marketing_start_date": "20161101"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (63187-784-90)", "package_ndc": "63187-784-90", "marketing_start_date": "20161101"}], "brand_name": "Dicyclomine Hydrochloride", "product_id": "63187-784_2bab7712-de3d-45a1-a21c-b6273721bb28", "dosage_form": "TABLET", "pharm_class": ["Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]"], "product_ndc": "63187-784", "generic_name": "Dicyclomine Hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dicyclomine Hydrochloride", "active_ingredients": [{"name": "DICYCLOMINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA085223", "marketing_category": "ANDA", "marketing_start_date": "19860730", "listing_expiration_date": "20261231"}