Product NDC: | 55154-4550 |
Proprietary Name: | Myambutol |
Non Proprietary Name: | Ethambutol Hydrochloride |
Active Ingredient(s): | 400 mg/1 & nbsp; Ethambutol Hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55154-4550 |
Labeler Name: | Cardinal Health |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA016320 |
Marketing Category: | NDA |
Start Marketing Date: | 20110627 |
Package NDC: | 55154-4550-0 |
Package Description: | 10 BLISTER PACK in 1 BAG (55154-4550-0) > 1 TABLET in 1 BLISTER PACK |
NDC Code | 55154-4550-0 |
Proprietary Name | Myambutol |
Package Description | 10 BLISTER PACK in 1 BAG (55154-4550-0) > 1 TABLET in 1 BLISTER PACK |
Product NDC | 55154-4550 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Ethambutol Hydrochloride |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20110627 |
Marketing Category Name | NDA |
Labeler Name | Cardinal Health |
Substance Name | ETHAMBUTOL HYDROCHLORIDE |
Strength Number | 400 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Antimycobacterial [EPC] |