dicyclomine hydrochloride

Generic: dicyclomine hydrochloride

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name dicyclomine hydrochloride
Generic Name dicyclomine hydrochloride
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

dicyclomine hydrochloride 20 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-2341
Product ID 71335-2341_8821239c-0d7f-4b89-90ba-554ca3e3d66a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040317
Listing Expiration 2026-12-31
Marketing Start 2023-04-25

Pharmacologic Class

Classes
anticholinergic [epc] cholinergic antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713352341
Hyphenated Format 71335-2341

Supplemental Identifiers

RxCUI
991086
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 ANDA040317 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71335-2341-1)
  • 40 TABLET in 1 BOTTLE (71335-2341-2)
  • 60 TABLET in 1 BOTTLE (71335-2341-3)
  • 90 TABLET in 1 BOTTLE (71335-2341-4)
  • 20 TABLET in 1 BOTTLE (71335-2341-5)
  • 21 TABLET in 1 BOTTLE (71335-2341-6)
  • 120 TABLET in 1 BOTTLE (71335-2341-7)
  • 100 TABLET in 1 BOTTLE (71335-2341-8)
  • 28 TABLET in 1 BOTTLE (71335-2341-9)
source: ndc

Packages (9)

71335-2341-1 30 TABLET in 1 BOTTLE (71335-2341-1) 71335-2341-2 40 TABLET in 1 BOTTLE (71335-2341-2) 71335-2341-3 60 TABLET in 1 BOTTLE (71335-2341-3) 71335-2341-4 90 TABLET in 1 BOTTLE (71335-2341-4) 71335-2341-5 20 TABLET in 1 BOTTLE (71335-2341-5) 71335-2341-6 21 TABLET in 1 BOTTLE (71335-2341-6) 71335-2341-7 120 TABLET in 1 BOTTLE (71335-2341-7) 71335-2341-8 100 TABLET in 1 BOTTLE (71335-2341-8) 71335-2341-9 28 TABLET in 1 BOTTLE (71335-2341-9)

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": "8821239c-0d7f-4b89-90ba-554ca3e3d66a", "openfda": {"unii": ["CQ903KQA31"], "rxcui": ["991086"], "spl_set_id": ["226a3a6e-9419-448a-827f-01199b792762"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-2341-1)", "package_ndc": "71335-2341-1", "marketing_start_date": "20240206"}, {"sample": false, "description": "40 TABLET in 1 BOTTLE (71335-2341-2)", "package_ndc": "71335-2341-2", "marketing_start_date": "20240206"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-2341-3)", "package_ndc": "71335-2341-3", "marketing_start_date": "20240206"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-2341-4)", "package_ndc": "71335-2341-4", "marketing_start_date": "20240206"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (71335-2341-5)", "package_ndc": "71335-2341-5", "marketing_start_date": "20240206"}, {"sample": false, "description": "21 TABLET in 1 BOTTLE (71335-2341-6)", "package_ndc": "71335-2341-6", "marketing_start_date": "20240206"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (71335-2341-7)", "package_ndc": "71335-2341-7", "marketing_start_date": "20240206"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-2341-8)", "package_ndc": "71335-2341-8", "marketing_start_date": "20240206"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (71335-2341-9)", "package_ndc": "71335-2341-9", "marketing_start_date": "20240206"}], "brand_name": "Dicyclomine Hydrochloride", "product_id": "71335-2341_8821239c-0d7f-4b89-90ba-554ca3e3d66a", "dosage_form": "TABLET", "pharm_class": ["Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]"], "product_ndc": "71335-2341", "generic_name": "Dicyclomine Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dicyclomine Hydrochloride", "active_ingredients": [{"name": "DICYCLOMINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA040317", "marketing_category": "ANDA", "marketing_start_date": "20230425", "listing_expiration_date": "20261231"}