Methylphenidate Hydrochloride marketed by Dr.Reddys Laboratories Inc under NDC Code 43598-438-01
NDC Code(s) : 43598-438-01, 43598-439-01, 43598-440-01, 43598-441-01
Packager : Dr.Reddys Laboratories Inc
Category : HUMAN PRESCRIPTION DRUG LABEL
DEA Schedule : CII
Marketing Status : New Drug Application
INGREDIENTS AND APPEARANCE
Methylphenidate HydrochlorideMethylphenidate Hydrochloride TABLET, EXTENDED RELEASE |
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Methylphenidate HydrochlorideMethylphenidate Hydrochloride TABLET, EXTENDED RELEASE |
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Methylphenidate HydrochlorideMethylphenidate Hydrochloride TABLET, EXTENDED RELEASE |
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Methylphenidate HydrochlorideMethylphenidate Hydrochloride TABLET, EXTENDED RELEASE |
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PRINCIPAL DISPLAY PANEL
Methylphenidate Hydrochloride Extended-Release Tablets USP, 18 mg - 100's Count
PRINCIPAL DISPLAY PANEL
Methylphenidate Hydrochloride Extended-Release Tablets USP, 27 mg - 100's Count
PRINCIPAL DISPLAY PANEL
Methylphenidate Hydrochloride Extended-Release Tablets USP, 36 mg - 100's Count
PRINCIPAL DISPLAY PANEL
Methylphenidate Hydrochloride Extended-Release Tablets USP, 54 mg - 100's Count
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