solifenacin succinate
Generic: solifenacin succinate
Labeler: alembic pharmaceuticals limitedDrug Facts
Product Profile
Brand Name
solifenacin succinate
Generic Name
solifenacin succinate
Labeler
alembic pharmaceuticals limited
Dosage Form
TABLET, COATED
Routes
Active Ingredients
solifenacin succinate 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
46708-193
Product ID
46708-193_aea71cde-6d62-4f8d-b813-47064cb213d9
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA205575
Listing Expiration
2026-12-31
Marketing Start
2019-05-20
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
46708193
Hyphenated Format
46708-193
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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
ANDA205575 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 80 TABLET, COATED in 1 CARTON (46708-193-08)
- 30 TABLET, COATED in 1 BOTTLE (46708-193-30)
- 90 TABLET, COATED in 1 BOTTLE (46708-193-90)
- 1000 TABLET, COATED in 1 BOTTLE (46708-193-91)
Packages (4)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "aea71cde-6d62-4f8d-b813-47064cb213d9", "openfda": {"upc": ["0346708193300"], "unii": ["KKA5DLD701"], "rxcui": ["477367", "477372"], "spl_set_id": ["aea71cde-6d62-4f8d-b813-47064cb213d9"], "manufacturer_name": ["Alembic Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "80 TABLET, COATED in 1 CARTON (46708-193-08)", "package_ndc": "46708-193-08", "marketing_start_date": "20190520"}, {"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (46708-193-30)", "package_ndc": "46708-193-30", "marketing_start_date": "20190520"}, {"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (46708-193-90)", "package_ndc": "46708-193-90", "marketing_start_date": "20190520"}, {"sample": false, "description": "1000 TABLET, COATED in 1 BOTTLE (46708-193-91)", "package_ndc": "46708-193-91", "marketing_start_date": "20190520"}], "brand_name": "Solifenacin Succinate", "product_id": "46708-193_aea71cde-6d62-4f8d-b813-47064cb213d9", "dosage_form": "TABLET, COATED", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "46708-193", "generic_name": "Solifenacin Succinate", "labeler_name": "Alembic Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Solifenacin Succinate", "active_ingredients": [{"name": "SOLIFENACIN SUCCINATE", "strength": "10 mg/1"}], "application_number": "ANDA205575", "marketing_category": "ANDA", "marketing_start_date": "20190520", "listing_expiration_date": "20261231"}