Home
>
National Drug Code (NDC)
>
ISONIAZID
ISONIAZID - 16590-984-90 - (ISONIAZID)
Drug Information of ISONIAZID
| Product NDC: | 16590-984 |
| Proprietary Name: | ISONIAZID |
| Non Proprietary Name: | ISONIAZID |
| Active Ingredient(s): | 300 mg/1 & nbsp; ISONIAZID |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ISONIAZID
| Product NDC: | 16590-984 |
| Labeler Name: | STAT RX USA LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA080937 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20101020 |
Package Information of ISONIAZID
| Package NDC: | 16590-984-90 |
| Package Description: | 90 TABLET in 1 BOTTLE (16590-984-90) |
NDC Information of ISONIAZID
| NDC Code | 16590-984-90 |
| Proprietary Name | ISONIAZID |
| Package Description | 90 TABLET in 1 BOTTLE (16590-984-90) |
| Product NDC | 16590-984 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ISONIAZID |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20101020 |
| Marketing Category Name | ANDA |
| Labeler Name | STAT RX USA LLC |
| Substance Name | ISONIAZID |
| Strength Number | 300 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Antimycobacterial [EPC] |
