Flavoxate Hydrochloride

Product NDC
51224-154
11-digit product format
512240154
Labeler code
51224
Product ID
51224-154_f3fe09d9-1537-40f4-aaab-627a7e05e149
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Flavoxate hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
TAGI Pharma, Inc.
Application
ANDA076835
Marketing category
ANDA
Marketing start
2011-03-25
Marketing end
2020-03-31
Substance
FLAVOXATE HYDROCHLORIDE
Active strength
100 mg/1
Pharmacologic classes
Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
51224-154-50EA - Each51224-154da0ca5dc-9e37-4122-8965-4d96d4260b7712012-07-24

DailyMed Socrata Ingredients#

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1095229flavoxATE HCl 100 MG Oral TabletPSNe05f4892-0be8-4178-a274-3289edca01371
1095229flavoxate hydrochloride 100 MG Oral TabletSCDe05f4892-0be8-4178-a274-3289edca01371