NDC 46708-386 – Modafinil

Modafinil 200 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV

Product NDC46708-386

Product details

Brand name
Modafinil
Generic name
Modafinil
Labeler
Alembic Pharmaceuticals Limited
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA202700
Marketed since
June 30, 2017
Listing expires
December 31, 2026
Pharmacologic class
Sympathomimetic-like Agent

Active ingredients

Uses, dosage, side effects and warnings for Modafinil →

Package NDC codes (5)

Package NDCDescriptionSince
46708-386-10100 TABLET in 1 CARTON (46708-386-10)Jun 30, 2017
46708-386-3030 TABLET in 1 BOTTLE (46708-386-30)Jun 30, 2017
46708-386-6060 TABLET in 1 BOTTLE (46708-386-60)Jun 30, 2017
46708-386-9090 TABLET in 1 BOTTLE (46708-386-90)Jun 30, 2017
46708-386-911000 TABLET in 1 BOTTLE (46708-386-91)Jun 30, 2017

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