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AMMONIUM LACTATE

ANDA · Abbreviated New Drug Application (Generic) · Sponsor: SUN PHARMA CANADA · Approved 2003-04-10

Drug application

FDA Application #
ANDA075883
Application type
Abbreviated New Drug Application (Generic)
Brand name
AMMONIUM LACTATE
Generic name
AMMONIUM LACTATE
Active ingredients
AMMONIUM LACTATE
Dosage form
CREAM
Route
TOPICAL
Marketing status
Prescription
Sponsor
SUN PHARMA CANADA
Manufacturer
Sun Pharmaceutical Industries, Inc.
First approval
2003-04-10

Source

Authoritative
Drugs@FDA application overview
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