Ethambutol Hydrochloride
Ethambutol Hydrochloride TABLETS USP 100 mg and 400 mg
Approved
Approval ID
55a70cf5-c4b5-450e-9fc5-129077dfdfd6
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Feb 5, 2021
Manufacturers
FDA
A-S Medication Solutions
DUNS: 830016429
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Ethambutol Hydrochloride
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code50090-2337
Application NumberNDA016320
Product Classification
M
Marketing Category
C73605
G
Generic Name
Ethambutol Hydrochloride
Product Specifications
Route of AdministrationORAL
Effective DateMay 16, 2019
FDA Product Classification
INGREDIENTS (9)
GELATIN, UNSPECIFIEDInactive
Code: 2G86QN327L
Classification: IACT
HYDROXYPROPYL CELLULOSE (1600000 WAMW)Inactive
Code: RFW2ET671P
Classification: IACT
SODIUM LAURYL SULFATEInactive
Code: 368GB5141J
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
SUCROSEInactive
Code: C151H8M554
Classification: IACT
TITANIUM DIOXIDEInactive
Code: 15FIX9V2JP
Classification: IACT
STEARIC ACIDInactive
Code: 4ELV7Z65AP
Classification: IACT
SORBITOLInactive
Code: 506T60A25R
Classification: IACT
ETHAMBUTOL HYDROCHLORIDEActive
Quantity: 100 mg in 1 1
Code: QE4VW5FO07
Classification: ACTIB