NDC 47335-326 – Naltrexone Hydrochloride

Naltrexone Hydrochloride 50 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC47335-326

Product details

Brand name
Naltrexone Hydrochloride
Generic name
Naltrexone Hydrochloride
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090356
Marketed since
February 29, 2012
Listing expires
December 31, 2027
Pharmacologic class
Opioid Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Naltrexone Hydrochloride →

Package NDC codes (4)

Package NDCDescriptionSince
47335-326-08100 TABLET, FILM COATED in 1 BOTTLE (47335-326-08)Feb 29, 2012
47335-326-181000 TABLET, FILM COATED in 1 BOTTLE (47335-326-18)Feb 29, 2012
47335-326-8330 TABLET, FILM COATED in 1 BOTTLE (47335-326-83)Feb 29, 2012
47335-326-88100 TABLET, FILM COATED in 1 BOTTLE (47335-326-88)Feb 29, 2012

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