Potassium Citrate Citric Acid Crystals

Product NDC
76439-261
11-digit product format
764390261
Labeler code
76439
Product ID
76439-261_b2bd2892-f42f-436e-bff2-0290f51704da
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Potassium Citrate and Citric Acid
Dosage form
GRANULE, FOR SOLUTION
Route
ORAL
Labeler
Virtus Pharmaceuticals LLC
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2014-06-13
Marketing end
2019-04-30
Substance
POTASSIUM CITRATE; CITRIC ACID MONOHYDRATE
Active strength
3 g/1; g/1
Pharmacologic classes
Acidifying Activity [MoA],Calculi Dissolution Agent [EPC],Anti-coagulant [EPC],Decreased Coagulation Factor Activity [PE],Calcium Chelating Activity [MoA],Acidifying Activity [MoA],Calculi Dissolution Agent [EPC],Anti-coagulant [EPC],Decreased Coagulation Factor Activity [PE],Calcium Chelating Activity [MoA]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
76439-261-10EA - Each76439-26124a6db3d-d10b-4c0c-aea0-2db430a252fd12014-08-01