NDC 70752-131 – Methylphenidate Hydrochloride

Methylphenidate Hydrochloride 5 mg/5mL · Solution · Oral

Human Prescription Drug DEA schedule CII

Product NDC70752-131

Product details

Brand name
Methylphenidate Hydrochloride
Generic name
Methylphenidate Hydrochloride
Labeler
QUAGEN PHARMACEUTICALS LLC
Dosage form
Solution
Route
Oral
Marketing category
ANDA · ANDA213567
Marketed since
June 4, 2020
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 (1)

Package NDCDescriptionSince
70752-131-14500 mL in 1 BOTTLE, PLASTIC (70752-131-14)Jun 4, 2020

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