NDC 67877-616 – Methylphenidate Hydrochloride

Methylphenidate Hydrochloride 5 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC67877-616

Product details

Brand name
Methylphenidate Hydrochloride
Generic name
Methylphenidate Hydrochloride
Labeler
Ascend Laboratories, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA211779
Marketed since
October 6, 2019
Listing expires
December 31, 2026
Pharmacologic class
Central Nervous System Stimulant

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
67877-616-01100 TABLET in 1 BOTTLE (67877-616-01)Oct 6, 2019
67877-616-3310 BLISTER PACK in 1 CARTON (67877-616-33) / 1 TABLET in 1 BLISTER PACKOct 6, 2019

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