Product NDC: | 60429-538 |
Proprietary Name: | Methylin |
Non Proprietary Name: | Methylphenidate Hydrochloride |
Active Ingredient(s): | 20 mg/1 & nbsp; Methylphenidate Hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 60429-538 |
Labeler Name: | Golden State Medical Supply, Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA040300 |
Marketing Category: | ANDA |
Start Marketing Date: | 20100520 |
Package NDC: | 60429-538-10 |
Package Description: | 1000 TABLET in 1 BOTTLE (60429-538-10) |
NDC Code | 60429-538-10 |
Proprietary Name | Methylin |
Package Description | 1000 TABLET in 1 BOTTLE (60429-538-10) |
Product NDC | 60429-538 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Methylphenidate Hydrochloride |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20100520 |
Marketing Category Name | ANDA |
Labeler Name | Golden State Medical Supply, Inc |
Substance Name | METHYLPHENIDATE HYDROCHLORIDE |
Strength Number | 20 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE] |