Home
>
National Drug Code (NDC)
>
Isoniazid
Isoniazid - 52959-145-81 - (Isoniazid)
Drug Information of Isoniazid
| Product NDC: | 52959-145 |
| 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: | 52959-145 |
| Labeler Name: | H.J. Harkins Company, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA087425 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19810714 |
Package Information of Isoniazid
| Package NDC: | 52959-145-81 |
| Package Description: | 180 TABLET in 1 BOTTLE (52959-145-81) |
NDC Information of Isoniazid
| NDC Code | 52959-145-81 |
| Proprietary Name | Isoniazid |
| Package Description | 180 TABLET in 1 BOTTLE (52959-145-81) |
| Product NDC | 52959-145 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Isoniazid |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19810714 |
| Marketing Category Name | ANDA |
| Labeler Name | H.J. Harkins Company, Inc. |
| Substance Name | ISONIAZID |
| Strength Number | 300 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Antimycobacterial [EPC] |
