diphenoxylate hydrochloride and atropine sulfate

Generic: diphenoxylate hydrochloride and atropine sulfate

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

Drug Facts

Product Profile

Brand Name diphenoxylate hydrochloride and atropine sulfate
Generic Name diphenoxylate hydrochloride and atropine sulfate
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

atropine sulfate .025 mg/1, diphenoxylate hydrochloride 2.5 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 72162-1765
Product ID 72162-1765_c4ae838c-25be-44fe-a54f-03495568e258
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA086727
DEA Schedule cv
Listing Expiration 2026-12-31
Marketing Start 2017-07-07

Pharmacologic Class

Classes
anticholinergic [epc] antidiarrheal [epc] cholinergic antagonists [moa] cholinergic muscarinic antagonist [epc] cholinergic muscarinic antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 721621765
Hyphenated Format 72162-1765

Supplemental Identifiers

RxCUI
1190572
UNII
03J5ZE7KA5 W24OD7YW48

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 diphenoxylate hydrochloride and atropine sulfate (source: ndc)
Generic Name diphenoxylate hydrochloride and atropine sulfate (source: ndc)
Application Number ANDA086727 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .025 mg/1
  • 2.5 mg/1
source: ndc
Packaging
  • 1000 TABLET in 1 BOTTLE (72162-1765-0)
  • 100 TABLET in 1 BOTTLE (72162-1765-1)
source: ndc

Packages (2)

72162-1765-0 1000 TABLET in 1 BOTTLE (72162-1765-0) 72162-1765-1 100 TABLET in 1 BOTTLE (72162-1765-1)

Ingredients (2)

atropine sulfate (.025 mg/1) diphenoxylate hydrochloride (2.5 mg/1)

Linked Drug Pages (1)

Diphenoxylate Hydrochloride and Atropine Sulfate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c4ae838c-25be-44fe-a54f-03495568e258", "openfda": {"unii": ["03J5ZE7KA5", "W24OD7YW48"], "rxcui": ["1190572"], "spl_set_id": ["c69408c2-ccb6-40b1-ae48-e033831c29aa"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (72162-1765-0)", "package_ndc": "72162-1765-0", "marketing_start_date": "20240201"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-1765-1)", "package_ndc": "72162-1765-1", "marketing_start_date": "20240201"}], "brand_name": "Diphenoxylate Hydrochloride and Atropine Sulfate", "product_id": "72162-1765_c4ae838c-25be-44fe-a54f-03495568e258", "dosage_form": "TABLET", "pharm_class": ["Anticholinergic [EPC]", "Antidiarrheal [EPC]", "Cholinergic Antagonists [MoA]", "Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "72162-1765", "dea_schedule": "CV", "generic_name": "Diphenoxylate Hydrochloride and Atropine Sulfate", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diphenoxylate Hydrochloride and Atropine Sulfate", "active_ingredients": [{"name": "ATROPINE SULFATE", "strength": ".025 mg/1"}, {"name": "DIPHENOXYLATE HYDROCHLORIDE", "strength": "2.5 mg/1"}], "application_number": "ANDA086727", "marketing_category": "ANDA", "marketing_start_date": "20170707", "listing_expiration_date": "20261231"}