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Ethambutol Hydrochloride
Ethambutol Hydrochloride - 54879-001-01 - (Ethambutol Hydrochloride)
Drug Information of Ethambutol Hydrochloride
| Product NDC: | 54879-001 |
| Proprietary Name: | Ethambutol Hydrochloride |
| Non Proprietary Name: | Ethambutol Hydrochloride |
| Active Ingredient(s): | 100 mg/1 & nbsp; Ethambutol Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ethambutol Hydrochloride
| Product NDC: | 54879-001 |
| Labeler Name: | STI Pharma LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA016320 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20061215 |
Package Information of Ethambutol Hydrochloride
| Package NDC: | 54879-001-01 |
| Package Description: | 12 CARTON in 1 BOX (54879-001-01) > 12 BOTTLE in 1 CARTON > 100 TABLET, FILM COATED in 1 BOTTLE |
NDC Information of Ethambutol Hydrochloride
| NDC Code | 54879-001-01 |
| Proprietary Name | Ethambutol Hydrochloride |
| Package Description | 12 CARTON in 1 BOX (54879-001-01) > 12 BOTTLE in 1 CARTON > 100 TABLET, FILM COATED in 1 BOTTLE |
| Product NDC | 54879-001 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ethambutol Hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20061215 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | STI Pharma LLC |
| Substance Name | ETHAMBUTOL HYDROCHLORIDE |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Antimycobacterial [EPC] |
