NDC 33342-087 – Rizatriptan

Rizatriptan Benzoate 5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 1 recall

Product NDC33342-087

Product details

Brand name
Rizatriptan
Generic name
Rizatriptan
Labeler
Macleods Pharmaceuticals Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA203147
Marketed since
March 11, 2014
Listing expires
December 31, 2026
Pharmacologic class
Serotonin-1b and Serotonin-1d Receptor Agonist

Active ingredients

Uses, dosage, side effects and warnings for Rizatriptan →

Package NDC codes (7)

Package NDCDescriptionSince
33342-087-0730 TABLET, FILM COATED in 1 CONTAINER (33342-087-07)Mar 11, 2014
33342-087-1210 BLISTER PACK in 1 CARTON (33342-087-12) / 10 TABLET, FILM COATED in 1 BLISTER PACKMar 11, 2014
33342-087-413 BLISTER PACK in 1 CARTON (33342-087-41) / 6 TABLET, FILM COATED in 1 BLISTER PACK (33342-087-02)Sep 3, 2018
33342-087-452 BLISTER PACK in 1 CARTON (33342-087-45) / 6 TABLET, FILM COATED in 1 BLISTER PACK (33342-087-02)Sep 3, 2018
33342-087-46200 TABLET, FILM COATED in 1 CONTAINER (33342-087-46)Mar 11, 2014
33342-087-504 BLISTER PACK in 1 CARTON (33342-087-50) / 3 TABLET, FILM COATED in 1 BLISTER PACK (33342-087-52)Mar 11, 2014
33342-087-726 BLISTER PACK in 1 CARTON (33342-087-72) / 3 TABLET, FILM COATED in 1 BLISTER PACK (33342-087-52)Mar 11, 2014

Recalls mentioning this NDC

Other Rizatriptan products