NDC 43602-178 – Methylphenidate Hydrochloride

Methylphenidate 10 mg/5mL · Solution · Oral

Human Prescription Drug DEA schedule CII

Product NDC43602-178

Product details

Brand name
Methylphenidate Hydrochloride
Generic name
Methylphenidate Hydrochloride
Labeler
Ascent Pharmaceuticals, Inc.
Dosage form
Solution
Route
Oral
Marketing category
ANDA · ANDA207417
Marketed since
January 29, 2021
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
43602-178-05500 mL in 1 BOTTLE (43602-178-05)Jan 29, 2021
43602-178-25250 mL in 1 BOTTLE (43602-178-25)Jan 29, 2021

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