Famotidine

Product NDC
0615-4594
11-digit product format
006154594
Labeler code
0615
Product ID
0615-4594_c007c1bf-9f5c-4c09-a5bd-e2346d756998
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Famotidine
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
NCS HealthCare of KY, Inc dba Vangard Labs
Application
ANDA075511
Marketing category
ANDA
Marketing start
2010-04-30
Marketing end
0000-00-00
Substance
FAMOTIDINE
Active strength
40 mg/1
Pharmacologic classes
Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]
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
0615-4594-392021-05-18C16284748780-197449f38-c6e6-f6ea-e053-dbdaa90aa703446c5df3-438a-4b18-a8a7-a23bd1bd86d0
0615-4594-392019-11-13C16284748780-197449f38-c6e6-f6ea-e053-dbdaa90aa703446c5df3-438a-4b18-a8a7-a23bd1bd86d0