Midodrine Hydrochloride

Product NDC
0615-5647
11-digit product format
006155647
Labeler code
0615
Product ID
0615-5647_8da8c36d-8167-4eeb-a788-4d777bcff619
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Midodrine Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
NCS HealthCare of KY, Inc dba Vangard Labs
Application
ANDA076577
Marketing category
ANDA
Marketing start
2003-09-10
Marketing end
0000-00-00
Substance
MIDODRINE HYDROCHLORIDE
Active strength
5 mg/1
Pharmacologic classes
Adrenergic alpha-Agonists [MoA],alpha-Adrenergic Agonist [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
0615-5647-392021-06-23C16284748780-19d75b9d0-88b4-f424-e053-dadaa90a57ce76d71394-cbef-48e1-b99e-9a80bd5babfc
0615-5647-392020-01-31C16284748780-19d75b9d0-88b4-f424-e053-dadaa90a57ce76d71394-cbef-48e1-b99e-9a80bd5babfc