NDC 67877-657 – Dexmethylphenidate Hydrochloride

Dexmethylphenidate Hydrochloride 10 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC67877-657

Product details

Brand name
Dexmethylphenidate Hydrochloride
Generic name
Dexmethylphenidate Hydrochloride
Labeler
Ascend Laboratories, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA212631
Marketed since
July 21, 2019
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 (3)

Package NDCDescriptionSince
67877-657-01100 TABLET in 1 BOTTLE (67877-657-01)Jul 21, 2019
67877-657-05500 TABLET in 1 BOTTLE (67877-657-05)Jul 21, 2019
67877-657-3030 TABLET in 1 BOTTLE (67877-657-30)Jul 21, 2019

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