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AMMONIUM LACTATE

ANDA · Abbreviated New Drug Application (Generic) · Sponsor: SUN PHARMA CANADA · Approved 2004-05-28

Drug application

FDA Application #
ANDA076216
Application type
Abbreviated New Drug Application (Generic)
Brand name
AMMONIUM LACTATE
Generic name
AMMONIUM LACTATE
Active ingredients
AMMONIUM LACTATE
Dosage form
LOTION
Route
TOPICAL
Marketing status
Prescription
Sponsor
SUN PHARMA CANADA
Manufacturer
Sun Pharmaceutical Industries, Inc.
First approval
2004-05-28

Source

Authoritative
Drugs@FDA application overview
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