Solifenacin Succinate

Product NDC
71205-934
11-digit product format
712050934
Labeler code
71205
Product ID
71205-934_53c1701c-04cf-4256-9fe0-4c08490e4f30
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
solifenacin succinate
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Proficient Rx LP
Application
ANDA210281
Marketing category
ANDA
Marketing start
2020-11-22
Marketing end
0000-00-00
Substance
SOLIFENACIN SUCCINATE
Active strength
10 mg/1
Pharmacologic classes
Cholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
71205-934-30EA - Each71205-934c34a0f15-ca02-4937-b1b2-5954d3e387a912021-06-02
71205-934-60EA - Each71205-9348a3ebda6-bad9-4ed3-9925-77b1f742af5d12021-06-02
71205-934-90EA - Each71205-934f63672f8-e6ee-4dd7-9f94-dd048c48467812021-06-02

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71205-934SOLIFENACIN SUCCINATE (SOLIFENACIN SUCCIATE) TABLET, FILM COATED SOLIFENACIN SUCCINATE TABLET, FILM COATED [PROFICIENT RX LP]2Legacy NDC20220421_46ecfaf3-bd9a-40cc-95dc-ff8ef43a8518.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
71205-934-307120509343030 TABLET, FILM COATED in 1 BOTTLE (71205-934-30) 2021-03-190000-00-00NoNoCurrent
71205-934-607120509346060 TABLET, FILM COATED in 1 BOTTLE (71205-934-60) 2021-03-190000-00-00NoNoCurrent
71205-934-907120509349090 TABLET, FILM COATED in 1 BOTTLE (71205-934-90) 2021-03-190000-00-00NoNoCurrent