Potassium Chloride

Product NDC
0615-1318
11-digit product format
006151318
Labeler code
0615
Product ID
0615-1318_d281058f-5ff7-40d2-a872-03dc73896ec8
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Potassium
Dosage form
CAPSULE
Route
ORAL
Labeler
NCS HealthCare of KY, Inc dba Vangard Labs
Application
ANDA077419
Marketing category
ANDA
Marketing start
2008-06-02
Marketing end
0000-00-00
Substance
POTASSIUM CHLORIDE
Active strength
750 mg/1
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#