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NEXAVIR

Approved
Approval ID

06af24a7-5779-4ef9-a066-b78b52898457

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Feb 19, 2020

Manufacturers
FDA

Nexco Pharma

DUNS: 023524538

Products 1

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

liver derivative complex

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code10530-319
Product Classification
G
Generic Name
liver derivative complex
Product Specifications
Route of AdministrationINTRAMUSCULAR, SUBCUTANEOUS
Effective DateFebruary 19, 2020
FDA Product Classification

INGREDIENTS (5)

HYDROCHLORIC ACIDInactive
Code: QTT17582CB
Classification: IACT
PHENOLInactive
Code: 339NCG44TV
Classification: IACT
SODIUM HYDROXIDEInactive
Code: 55X04QC32I
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
PORK LIVERActive
Quantity: 25.5 mg in 1 mL
Code: 6EC706HI7F
Classification: ACTIB

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NEXAVIR - FDA Drug Approval Details