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NALTREXONE

ANDA · Abbreviated New Drug Application (Generic) · Sponsor: TEVA PHARMS USA INC · Approved 2023-07-06

Drug application

FDA Application #
ANDA213195
Application type
Abbreviated New Drug Application (Generic)
Brand name
NALTREXONE
Generic name
Naltrexone
Active ingredients
NALTREXONE
Dosage form
FOR SUSPENSION, EXTENDED RELEASE
Route
INTRAMUSCULAR
Marketing status
Discontinued
Sponsor
TEVA PHARMS USA INC
First approval
2023-07-06

Source

Authoritative
Drugs@FDA application overview
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