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Metronidazole

Metronidazole Vaginal Gel, 0.75% FOR INTRAVAGINAL USE ONLY NOT FOR OPHTHALMIC, DERMAL, OR ORAL USE

Approved
Approval ID

94a83daa-6e34-419d-849a-6f18d3b8c586

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Aug 14, 2023

Manufacturers
FDA

Solaris Pharma Corporation

DUNS: 079904672

Products 1

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

Metronidazole

PRODUCT DETAILS

NDC Product Code73473-303
Application NumberANDA213648
Marketing CategoryC73584
Route of AdministrationVAGINAL
Effective DateAugust 14, 2023
Generic NameMetronidazole

INGREDIENTS (1)

METRONIDAZOLEActive
Quantity: 7.5 mg in 1 g
Code: 140QMO216E
Classification: ACTIB

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Metronidazole - FDA Drug Approval Details