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Azithromycin Monohydrate

These highlights do not include all the information needed to use AZITHROMYCIN TABLETS safely and effectively. See full prescribing information for AZITHROMYCIN TABLETS. AZITHROMYCIN tablets, 250 mg and 500 mg, for oral use Initial U.S. Approval: 1991

Approved
Approval ID

62d64414-d3ab-1741-e053-2a91aa0ac0f8

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Jan 1, 2018

Manufacturers
FDA

MAS MANAGEMENT GROUP, INC.

DUNS: 079363782

Products 1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

Azithromycin Monohydrate

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code69677-129
Application NumberANDA065398
Product Classification
M
Marketing Category
C73584
G
Generic Name
Azithromycin Monohydrate
Product Specifications
Route of AdministrationORAL
Effective DateJanuary 1, 2018
FDA Product Classification

INGREDIENTS (10)

CALCIUM PHOSPHATE, DIBASIC, ANHYDROUSInactive
Code: L11K75P92J
Classification: IACT
HYPROMELLOSE 2910 (15 MPA.S)Inactive
Code: 36SFW2JZ0W
Classification: IACT
D&C RED NO. 30Inactive
Code: 2S42T2808B
Classification: IACT
CROSCARMELLOSE SODIUMInactive
Code: M28OL1HH48
Classification: IACT
TRIACETINInactive
Code: XHX3C3X673
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
LACTOSE MONOHYDRATEInactive
Code: EWQ57Q8I5X
Classification: IACT
SODIUM LAURYL SULFATEInactive
Code: 368GB5141J
Classification: IACT
TITANIUM DIOXIDEInactive
Code: 15FIX9V2JP
Classification: IACT
AZITHROMYCIN MONOHYDRATEActive
Quantity: 250 mg in 1 1
Code: JTE4MNN1MD
Classification: ACTIM

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Azithromycin Monohydrate - FDA Drug Approval Details