SARAFEM

Product NDC
0430-0220
11-digit product format
004300220
Labeler code
0430
Product ID
0430-0220_01dbb115-7a56-42c2-b6c9-d9ded44fab80
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
fluoxetine hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
Allergan, Inc.
Application
NDA021860
Marketing category
NDA
Marketing start
2008-06-24
Marketing end
0000-00-00
Substance
FLUOXETINE HYDROCHLORIDE
Active strength
20 mg/1
Pharmacologic classes
Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0430-0220-14EA - Each0430-02204b60afe4-18ce-44ba-8236-7c976eba699e12012-07-24

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0430-0220-14004300220144 BLISTER PACK in 1 CARTON (0430-0220-14) > 7 TABLET in 1 BLISTER PACK4 blister pack2008-06-240000-00-00NoNoCurrent