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Isoniazid
Isoniazid - 0555-0071-02 - (Isoniazid)
Drug Information of Isoniazid
| Product NDC: | 0555-0071 |
| 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: | 0555-0071 |
| Labeler Name: | Barr Laboratories Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA080937 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19720901 |
Package Information of Isoniazid
| Package NDC: | 0555-0071-02 |
| Package Description: | 100 TABLET in 1 BOTTLE (0555-0071-02) |
NDC Information of Isoniazid
| NDC Code | 0555-0071-02 |
| Proprietary Name | Isoniazid |
| Package Description | 100 TABLET in 1 BOTTLE (0555-0071-02) |
| Product NDC | 0555-0071 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Isoniazid |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19720901 |
| Marketing Category Name | ANDA |
| Labeler Name | Barr Laboratories Inc. |
| Substance Name | ISONIAZID |
| Strength Number | 300 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Antimycobacterial [EPC] |
