NDC 70010-007 – Dexmethylphenidate Hydrochloride

Dexmethylphenidate Hydrochloride 20 mg/1 · Capsule, Extended Release · Oral

Human Prescription Drug DEA schedule CII

Product NDC70010-007

Product details

Brand name
Dexmethylphenidate Hydrochloride
Generic name
Dexmethylphenidate Hydrochloride
Labeler
Granules Pharmaceuticals Inc.
Dosage form
Capsule, Extended Release
Route
Oral
Marketing category
ANDA · ANDA213813
Marketed since
December 1, 2020
Listing expires
December 31, 2026
Pharmacologic class
Central Nervous System Stimulant

Active ingredients

Uses, dosage, side effects and warnings for Dexmethylphenidate Hydrochloride →

Package NDC codes (1)

Package NDCDescriptionSince
70010-007-01100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70010-007-01)Dec 1, 2020

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