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Isoniazid
Isoniazid - 63629-1415-1 - (isoniazid)
Drug Information of Isoniazid
| Product NDC: | 63629-1415 |
| Proprietary Name: | Isoniazid |
| Non Proprietary Name: | isoniazid |
| Active Ingredient(s): | 50 mg/5mL & nbsp; isoniazid |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Isoniazid
| Product NDC: | 63629-1415 |
| Labeler Name: | Bryant Ranch Prepack |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA088235 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19831111 |
Package Information of Isoniazid
| Package NDC: | 63629-1415-1 |
| Package Description: | 240 mL in 1 BOTTLE (63629-1415-1) |
NDC Information of Isoniazid
| NDC Code | 63629-1415-1 |
| Proprietary Name | Isoniazid |
| Package Description | 240 mL in 1 BOTTLE (63629-1415-1) |
| Product NDC | 63629-1415 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | isoniazid |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 19831111 |
| Marketing Category Name | ANDA |
| Labeler Name | Bryant Ranch Prepack |
| Substance Name | ISONIAZID |
| Strength Number | 50 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Antimycobacterial [EPC] |
