Solifenacin Succinate

Product NDC
82804-044
11-digit product format
828040044
Labeler code
82804
Product ID
82804-044_8ab4f222-018f-40fc-a6aa-39dab563a8a0
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Solifenacin Succinate
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Proficient Rx LP
Application
ANDA211701
Marketing category
ANDA
Marketing start
2020-03-23
Substance
SOLIFENACIN SUCCINATE
Active strength
5 mg/1
Pharmacologic classes
Cholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
KKA5DLD701SOLIFENACIN SUCCINATE242478-38-2SOLIFENACIN SUCCINATE

Packages

Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
82804-044-308280400443030 TABLET, FILM COATED in 1 BOTTLE (82804-044-30) 2023-11-28NoNoHistorical
82804-044-608280400446060 TABLET, FILM COATED in 1 BOTTLE (82804-044-60) 2023-11-28NoNoHistorical
82804-044-908280400449090 TABLET, FILM COATED in 1 BOTTLE (82804-044-90) 2023-11-28NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Solifenacin SuccinateProficient Rx LP2023-11-01HUMAN PRESCRIPTION DRUG LABEL1