0591-3795
Generic: solifenacin succinate
Labeler: actavis pharma, inc.Drug Facts
Product Profile
Brand Name
Generic Name
solifenacin succinate
Labeler
actavis pharma, inc.
Dosage Form
TABLET, FILM COATED
Active Ingredients
solifenacin succinate 5 mg/1
Identifiers & Regulatory
Product NDC
0591-3795
Product ID
0591-3795_15086423-fd46-4928-90be-b5fdd8acf950
Product Type
DRUG FOR FURTHER PROCESSING
Marketing Category
DRUG FOR FURTHER PROCESSING
Marketing Start
2019-09-27
Marketing End
2026-05-31
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
05913795
Hyphenated Format
0591-3795
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: label)
Generic Name
solifenacin succinate (source: ndc)
Application Number
ANDA202551 (source: label)
Routes
source: label
Resolved Composition
Strengths
- 5 mg/1
Packaging
- 97087 TABLET, FILM COATED in 1 BOX (0591-3795-00)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"spl_id": "15086423-fd46-4928-90be-b5fdd8acf950", "openfda": {}, "finished": false, "packaging": [{"description": "97087 TABLET, FILM COATED in 1 BOX (0591-3795-00)", "package_ndc": "0591-3795-00", "marketing_end_date": "31-MAY-26", "marketing_start_date": "27-SEP-19"}], "product_id": "0591-3795_15086423-fd46-4928-90be-b5fdd8acf950", "dosage_form": "TABLET, FILM COATED", "product_ndc": "0591-3795", "generic_name": "solifenacin succinate", "labeler_name": "Actavis Pharma, Inc.", "product_type": "DRUG FOR FURTHER PROCESSING", "brand_name_base": null, "active_ingredients": [{"name": "SOLIFENACIN SUCCINATE", "strength": "5 mg/1"}], "marketing_category": "DRUG FOR FURTHER PROCESSING", "marketing_end_date": "20260531", "marketing_start_date": "20190927"}