NDC 68382-188 – Dipyridamole

Dipyridamole 50 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC68382-188

Product details

Brand name
Dipyridamole
Generic name
Dipyridamole
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA040874
Marketed since
May 22, 2008
Listing expires
December 31, 2026
Pharmacologic class
Platelet Aggregation Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Dipyridamole →

Package NDC codes (4)

Package NDCDescriptionSince
68382-188-01100 TABLET, FILM COATED in 1 BOTTLE (68382-188-01)May 22, 2008
68382-188-05500 TABLET, FILM COATED in 1 BOTTLE (68382-188-05)May 22, 2008
68382-188-101000 TABLET, FILM COATED in 1 BOTTLE (68382-188-10)May 22, 2008
68382-188-7710 BLISTER PACK in 1 CARTON (68382-188-77) / 10 TABLET, FILM COATED in 1 BLISTER PACKMay 22, 2008

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