Methylphenidate Hydrochloride (CD) - NDC drug/product
NDCs and labelers of "Methylphenidate Hydrochloride (CD)":
NDC | Trade Name | Labeler Name | Deleted | Deleted Date |
---|---|---|---|---|
60687-0140 | Methylphenidate Hydrochloride (CD) | American Health Packaging | YES | 2018-08-31 |
60687-0151 | Methylphenidate Hydrochloride (CD) | American Health Packaging | YES | 2018-08-31 |
00093-5292 | Methylphenidate Hydrochloride (CD) | Teva Pharmaceuticals USA, Inc. | YES | 2024-10-31 |
00093-5293 | Methylphenidate Hydrochloride (CD) | Teva Pharmaceuticals USA, Inc. | YES | 2024-10-31 |
00093-5295 | Methylphenidate Hydrochloride (CD) | Teva Pharmaceuticals USA, Inc. | NO | |
00093-5296 | Methylphenidate Hydrochloride (CD) | Teva Pharmaceuticals USA, Inc. | NO | |
00093-5297 | Methylphenidate Hydrochloride (CD) | Teva Pharmaceuticals USA, Inc. | NO | |
00093-5298 | Methylphenidate Hydrochloride (CD) | Teva Pharmaceuticals USA, Inc. | YES | 2024-10-31 |
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