darifenacin
Generic: darifenacin
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
darifenacin
Generic Name
darifenacin
Labeler
bryant ranch prepack
Dosage Form
TABLET, EXTENDED RELEASE
Routes
Active Ingredients
darifenacin hydrobromide 7.5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72162-2570
Product ID
72162-2570_2a6e97d9-19e4-42aa-86e8-27bab91f059d
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA205209
Listing Expiration
2026-12-31
Marketing Start
2016-11-18
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
721622570
Hyphenated Format
72162-2570
Supplemental Identifiers
RxCUI
UNII
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
darifenacin (source: ndc)
Generic Name
darifenacin (source: ndc)
Application Number
ANDA205209 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 7.5 mg/1
Packaging
- 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-2570-3)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2a6e97d9-19e4-42aa-86e8-27bab91f059d", "openfda": {"unii": ["CR02EYQ8GV"], "rxcui": ["485423"], "spl_set_id": ["697eba55-9e1f-4036-baed-5644c810f166"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-2570-3)", "package_ndc": "72162-2570-3", "marketing_start_date": "20251117"}], "brand_name": "Darifenacin", "product_id": "72162-2570_2a6e97d9-19e4-42aa-86e8-27bab91f059d", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "72162-2570", "generic_name": "Darifenacin", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Darifenacin", "active_ingredients": [{"name": "DARIFENACIN HYDROBROMIDE", "strength": "7.5 mg/1"}], "application_number": "ANDA205209", "marketing_category": "ANDA", "marketing_start_date": "20161118", "listing_expiration_date": "20261231"}