NDC 68382-113 – risperidone

Risperidone .5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC68382-113

Product details

Brand name
risperidone
Generic name
risperidone
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078040
Marketed since
November 13, 2008
Listing expires
December 31, 2026
Pharmacologic class
Atypical Antipsychotic

Active ingredients

Uses, dosage, side effects and warnings for Risperidone →

Package NDC codes (6)

Package NDCDescriptionSince
68382-113-01100 TABLET, FILM COATED in 1 BOTTLE (68382-113-01)Nov 13, 2008
68382-113-05500 TABLET, FILM COATED in 1 BOTTLE (68382-113-05)Nov 13, 2008
68382-113-0630 TABLET, FILM COATED in 1 BOTTLE (68382-113-06)Nov 13, 2008
68382-113-101000 TABLET, FILM COATED in 1 BOTTLE (68382-113-10)Nov 13, 2008
68382-113-1460 TABLET, FILM COATED in 1 BOTTLE (68382-113-14)Nov 13, 2008
68382-113-1690 TABLET, FILM COATED in 1 BOTTLE (68382-113-16)Nov 13, 2008

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