solifenacin succinate

Generic: solifenacin succinate

Labeler: camber pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name solifenacin succinate
Generic Name solifenacin succinate
Labeler camber pharmaceuticals, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

solifenacin succinate 10 mg/1

Manufacturer
Camber Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 31722-028
Product ID 31722-028_e52cdf06-9178-ab2f-e053-2a95a90af2b3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA215761
Listing Expiration 2026-12-31
Marketing Start 2022-06-15

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 31722028
Hyphenated Format 31722-028

Supplemental Identifiers

RxCUI
477367 477372
UPC
0331722028301 0331722027908 0331722027304 0331722028905
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 ANDA215761 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (31722-028-30)
  • 10 BLISTER PACK in 1 CARTON (31722-028-31) / 10 TABLET, FILM COATED in 1 BLISTER PACK (31722-028-32)
  • 90 TABLET, FILM COATED in 1 BOTTLE (31722-028-90)
source: ndc

Packages (3)

31722-028-30 30 TABLET, FILM COATED in 1 BOTTLE (31722-028-30) 31722-028-31 10 BLISTER PACK in 1 CARTON (31722-028-31) / 10 TABLET, FILM COATED in 1 BLISTER PACK (31722-028-32) 31722-028-90 90 TABLET, FILM COATED in 1 BOTTLE (31722-028-90)

Ingredients (1)

solifenacin succinate (10 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": "e52cdf06-9178-ab2f-e053-2a95a90af2b3", "openfda": {"upc": ["0331722028301", "0331722027908", "0331722027304", "0331722028905"], "unii": ["KKA5DLD701"], "rxcui": ["477367", "477372"], "spl_set_id": ["6479d24f-373e-4c9e-abaf-349f90a2bbb1"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (31722-028-30)", "package_ndc": "31722-028-30", "marketing_start_date": "20220615"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (31722-028-31)  / 10 TABLET, FILM COATED in 1 BLISTER PACK (31722-028-32)", "package_ndc": "31722-028-31", "marketing_start_date": "20220615"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (31722-028-90)", "package_ndc": "31722-028-90", "marketing_start_date": "20220615"}], "brand_name": "solifenacin succinate", "product_id": "31722-028_e52cdf06-9178-ab2f-e053-2a95a90af2b3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "31722-028", "generic_name": "solifenacin succinate", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "solifenacin succinate", "active_ingredients": [{"name": "SOLIFENACIN SUCCINATE", "strength": "10 mg/1"}], "application_number": "ANDA215761", "marketing_category": "ANDA", "marketing_start_date": "20220615", "listing_expiration_date": "20261231"}