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Myambutol
Myambutol - 68850-012-02 - (Ethambutol hydrochloride)
Drug Information of Myambutol
| Product NDC: | 68850-012 |
| 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, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Myambutol
| Product NDC: | 68850-012 |
| Labeler Name: | STI Pharma, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA016320 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20070810 |
Package Information of Myambutol
| Package NDC: | 68850-012-02 |
| Package Description: | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (68850-012-02) > 10 TABLET, FILM COATED in 1 BLISTER PACK |
NDC Information of Myambutol
| NDC Code | 68850-012-02 |
| Proprietary Name | Myambutol |
| Package Description | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (68850-012-02) > 10 TABLET, FILM COATED in 1 BLISTER PACK |
| Product NDC | 68850-012 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ethambutol hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20070810 |
| Marketing Category Name | NDA |
| Labeler Name | STI Pharma, LLC |
| Substance Name | ETHAMBUTOL HYDROCHLORIDE |
| Strength Number | 400 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Antimycobacterial [EPC] |
