dicyclomine hydrochloride

Generic: dicyclomine hydrochloride

Labeler: camber pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name dicyclomine hydrochloride
Generic Name dicyclomine hydrochloride
Labeler camber pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

dicyclomine hydrochloride 20 mg/1

Manufacturer
Camber Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 31722-079
Product ID 31722-079_24d1b166-e43d-91de-e063-6394a90ae579
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217566
Listing Expiration 2026-12-31
Marketing Start 2024-05-07

Pharmacologic Class

Classes
anticholinergic [epc] cholinergic antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 31722079
Hyphenated Format 31722-079

Supplemental Identifiers

RxCUI
991086
UPC
0331722079013 0331722079105
UNII
CQ903KQA31

Packaging Origin

Original Packager
true

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 ANDA217566 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (31722-079-01)
  • 1000 TABLET in 1 BOTTLE (31722-079-10)
source: ndc

Packages (2)

31722-079-01 100 TABLET in 1 BOTTLE (31722-079-01) 31722-079-10 1000 TABLET in 1 BOTTLE (31722-079-10)

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": "24d1b166-e43d-91de-e063-6394a90ae579", "openfda": {"upc": ["0331722079013", "0331722079105"], "unii": ["CQ903KQA31"], "rxcui": ["991086"], "spl_set_id": ["0590c805-537e-46d3-9500-f4942c1df2ea"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (31722-079-01)", "package_ndc": "31722-079-01", "marketing_start_date": "20240507"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (31722-079-10)", "package_ndc": "31722-079-10", "marketing_start_date": "20240507"}], "brand_name": "Dicyclomine hydrochloride", "product_id": "31722-079_24d1b166-e43d-91de-e063-6394a90ae579", "dosage_form": "TABLET", "pharm_class": ["Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]"], "product_ndc": "31722-079", "generic_name": "Dicyclomine hydrochloride", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dicyclomine hydrochloride", "active_ingredients": [{"name": "DICYCLOMINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA217566", "marketing_category": "ANDA", "marketing_start_date": "20240507", "listing_expiration_date": "20261231"}