TRANYLCYPROMINE SULFATE

Product NDC
49884-032
11-digit product format
498840032
Labeler code
49884
Product ID
49884-032_dbe61ac0-e4b2-47e4-aa72-048e86a0b984
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
tranylcypromine sulfate
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Par Pharmaceutical, Inc.
Application
ANDA040640
Marketing category
ANDA
Marketing start
2006-06-30
Marketing end
2024-11-30
Substance
TRANYLCYPROMINE SULFATE
Active strength
10 mg/1
Pharmacologic classes
Monoamine Oxidase Inhibitor [EPC], Monoamine Oxidase Inhibitors [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
49884-032-01EA - Each49884-03284ba4663-f579-4476-a2d6-ec96bfbddfae12012-07-24

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
49884-032-0149884003201100 TABLET, FILM COATED in 1 BOTTLE (49884-032-01) 2006-06-300000-00-00NoNoCurrent