Cyproheptadine Hydrochloride

Product NDC
0615-1536
11-digit product format
006151536
Labeler code
0615
Product ID
0615-1536_4a02f757-be72-4d37-b1a1-a6d8fd716fd7
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Cyproheptadine Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
NCS HealthCare of KY, Inc dba Vangard Labs
Application
ANDA087056
Marketing category
ANDA
Marketing start
2010-01-08
Marketing end
0000-00-00
Substance
CYPROHEPTADINE HYDROCHLORIDE
Active strength
4 mg/1
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0615-1536-392021-04-12C16284748780-19d75b9cf-d9f1-f424-e053-dadaa90a57ce8d2bd313-3ab3-4fed-81d6-d2d81edcb206
0615-1536-392020-01-31C16284748780-19d75b9cf-d9f1-f424-e053-dadaa90a57ce8d2bd313-3ab3-4fed-81d6-d2d81edcb206