Methylphenidate Hydrochloride (CD)  - NDC drug/product


NDCs and labelers of "Methylphenidate Hydrochloride (CD)":

NDCTrade NameLabeler NameDeletedDeleted Date
60687-0140Methylphenidate Hydrochloride (CD)American Health PackagingYES2018-08-31
60687-0151Methylphenidate Hydrochloride (CD)American Health PackagingYES2018-08-31
00093-5292Methylphenidate Hydrochloride (CD)Teva Pharmaceuticals USA, Inc.YES2024-10-31
00093-5293Methylphenidate Hydrochloride (CD)Teva Pharmaceuticals USA, Inc.YES2024-10-31
00093-5295Methylphenidate Hydrochloride (CD)Teva Pharmaceuticals USA, Inc.YES2025-04-30
00093-5296Methylphenidate Hydrochloride (CD)Teva Pharmaceuticals USA, Inc.YESNo later than 2024-12-19
00093-5297Methylphenidate Hydrochloride (CD)Teva Pharmaceuticals USA, Inc.YES2025-04-30
00093-5298Methylphenidate Hydrochloride (CD)Teva Pharmaceuticals USA, Inc.YES2024-10-31
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