CYPROHEPTADINE HYDROCHLORIDE

Product NDC
71335-0758
11-digit product format
713350758
Labeler code
71335
Product ID
71335-0758_99e9fe13-d69f-4114-89d9-c6b8401943e1
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
CYPROHEPTADINE HYDROCHLORIDE
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA208938
Marketing category
ANDA
Marketing start
2017-07-20
Marketing end
0000-00-00
Substance
CYPROHEPTADINE HYDROCHLORIDE
Active strength
4 mg/1
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
71335-0758-1EA - Each71335-075860dec9e8-def1-4b15-978b-8df96f6ea4a512022-09-12

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71335-0758-17133507580130 TABLET in 1 BOTTLE (71335-0758-1) 30 tablet2018-04-020000-00-00NoNoCurrent
71335-0758-27133507580260 TABLET in 1 BOTTLE (71335-0758-2) 60 tablet2018-04-020000-00-00NoNoCurrent
71335-0758-37133507580328 TABLET in 1 BOTTLE (71335-0758-3) 28 tablet2018-04-020000-00-00NoNoCurrent
71335-0758-471335075804100 TABLET in 1 BOTTLE (71335-0758-4) 100 tablet2018-04-020000-00-00NoNoCurrent
71335-0758-57133507580590 TABLET in 1 BOTTLE (71335-0758-5) 90 tablet2018-04-020000-00-00NoNoCurrent