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NDC 00406-1146-10 Methylphenidate Hydrochloride 20 mg/1 Details
Methylphenidate Hydrochloride 20 mg/1
Methylphenidate Hydrochloride is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by SpecGx LLC. The primary component is METHYLPHENIDATE HYDROCHLORIDE.
Product Information
| NDC | 00406-1146 |
|---|---|
| Product ID | 0406-1146_6d75b224-bdfa-4f2b-9165-83a4e1a342e2 |
| Associated GPIs | 61400020100315 |
| GCN Sequence Number | 004027 |
| GCN Sequence Number Description | methylphenidate HCl TABLET 20 MG ORAL |
| HIC3 | H2V |
| HIC3 Description | TX FOR ATTENTION DEFICIT-HYPERACT(ADHD)/NARCOLEPSY |
| GCN | 15920 |
| HICL Sequence Number | 001682 |
| HICL Sequence Number Description | METHYLPHENIDATE HCL |
| Brand/Generic | Generic |
| Proprietary Name | Methylphenidate Hydrochloride |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Methylphenidate Hydrochloride |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 20 |
| Active Ingredient Units | mg/1 |
| Substance Name | METHYLPHENIDATE HYDROCHLORIDE |
| Labeler Name | SpecGx LLC |
| Pharmaceutical Class | Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE] |
| DEA Schedule | CII |
| Marketing Category | ANDA |
| Application Number | ANDA040300 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 00406-1146-10 (00406114610)
| NDC Package Code | 0406-1146-10 |
|---|---|
| Billing NDC | 00406114610 |
| Package | 1000 TABLET in 1 BOTTLE (0406-1146-10) |
| Marketing Start Date | 1998-11-27 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |