dicyclomine hydrochloride

Generic: dicyclomine hydrochloride

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name dicyclomine hydrochloride
Generic Name dicyclomine hydrochloride
Labeler american health packaging
Dosage Form TABLET
Routes
ORAL
Active Ingredients

dicyclomine hydrochloride 20 mg/1

Manufacturer
American Health Packaging

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
anticholinergic [epc] cholinergic antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60687380
Hyphenated Format 60687-380

Supplemental Identifiers

RxCUI
991061 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 ANDA040230 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-380-01) / 1 TABLET in 1 BLISTER PACK (60687-380-11)
source: ndc

Packages (1)

Ingredients (1)

dicyclomine hydrochloride (20 mg/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"}