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Isoniazid
Isoniazid - 0781-3056-70 - (Isoniazid)
Drug Information of Isoniazid
| Product NDC: | 0781-3056 |
| Proprietary Name: | Isoniazid |
| Non Proprietary Name: | Isoniazid |
| Active Ingredient(s): | 100 mg/mL & nbsp; Isoniazid |
| Administration Route(s): | INTRAMUSCULAR |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Isoniazid
| Product NDC: | 0781-3056 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040648 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20060119 |
Package Information of Isoniazid
| Package NDC: | 0781-3056-70 |
| Package Description: | 1 VIAL, MULTI-DOSE in 1 CARTON (0781-3056-70) > 10 mL in 1 VIAL, MULTI-DOSE |
NDC Information of Isoniazid
| NDC Code | 0781-3056-70 |
| Proprietary Name | Isoniazid |
| Package Description | 1 VIAL, MULTI-DOSE in 1 CARTON (0781-3056-70) > 10 mL in 1 VIAL, MULTI-DOSE |
| Product NDC | 0781-3056 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Isoniazid |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR |
| Start Marketing Date | 20060119 |
| Marketing Category Name | ANDA |
| Labeler Name | Sandoz Inc |
| Substance Name | ISONIAZID |
| Strength Number | 100 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Antimycobacterial [EPC] |
