solifenacin succinate

Generic: solifenacin succinate

Labeler: novadoz pharmaceuticals llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name solifenacin succinate
Generic Name solifenacin succinate
Labeler novadoz pharmaceuticals llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

solifenacin succinate 5 mg/1

Manufacturer
Novadoz Pharmaceuticals LLC

Identifiers & Regulatory

Product NDC 72205-020
Product ID 72205-020_eaccb7fc-2098-43d1-a64e-759b8d4c35c2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210688
Listing Expiration 2026-12-31
Marketing Start 2019-05-20

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72205020
Hyphenated Format 72205-020

Supplemental Identifiers

RxCUI
477367 477372
UPC
0372205021907 0372205020306 0372205021303 0372205020900
UNII
KKA5DLD701

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 solifenacin succinate (source: ndc)
Generic Name solifenacin succinate (source: ndc)
Application Number ANDA210688 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (72205-020-30)
  • 90 TABLET in 1 BOTTLE (72205-020-90)
  • 1000 TABLET in 1 BOTTLE (72205-020-99)
source: ndc

Packages (3)

72205-020-30 30 TABLET in 1 BOTTLE (72205-020-30) 72205-020-90 90 TABLET in 1 BOTTLE (72205-020-90) 72205-020-99 1000 TABLET in 1 BOTTLE (72205-020-99)

Ingredients (1)

solifenacin succinate (5 mg/1)

Linked Drug Pages (1)

Solifenacin Succinate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "eaccb7fc-2098-43d1-a64e-759b8d4c35c2", "openfda": {"upc": ["0372205021907", "0372205020306", "0372205021303", "0372205020900"], "unii": ["KKA5DLD701"], "rxcui": ["477367", "477372"], "spl_set_id": ["98b99a4c-201d-46ee-b78c-7634a64d3a8d"], "manufacturer_name": ["Novadoz Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72205-020-30)", "package_ndc": "72205-020-30", "marketing_start_date": "20190520"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (72205-020-90)", "package_ndc": "72205-020-90", "marketing_start_date": "20190520"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (72205-020-99)", "package_ndc": "72205-020-99", "marketing_start_date": "20190520"}], "brand_name": "Solifenacin Succinate", "product_id": "72205-020_eaccb7fc-2098-43d1-a64e-759b8d4c35c2", "dosage_form": "TABLET", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "72205-020", "generic_name": "Solifenacin Succinate", "labeler_name": "Novadoz Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Solifenacin Succinate", "active_ingredients": [{"name": "SOLIFENACIN SUCCINATE", "strength": "5 mg/1"}], "application_number": "ANDA210688", "marketing_category": "ANDA", "marketing_start_date": "20190520", "listing_expiration_date": "20261231"}