NDC 69238-1175 – Isotretinoin

Isotretinoin 20 mg/1 · Capsule, Liquid Filled · Oral

Human Prescription Drug 1 recall

Product NDC69238-1175

Product details

Brand name
Isotretinoin
Generic name
Isotretinoin
Labeler
Amneal Pharmaceuticals LLC
Dosage form
Capsule, Liquid Filled
Route
Oral
Marketing category
ANDA · ANDA207792
Marketed since
October 2, 2017
Listing expires
December 31, 2027
Pharmacologic class
Retinoid

Active ingredients

Uses, dosage, side effects and warnings for Isotretinoin →

Package NDC codes (1)

Package NDCDescriptionSince
69238-1175-33 BLISTER PACK in 1 CARTON (69238-1175-3) / 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (69238-1175-1)Oct 2, 2017

Recalls mentioning this NDC

Other Isotretinoin products