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Spotex

Spotex

Approved
Approval ID

d0485ea3-984d-3193-e053-2995a90a078f

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Dec 26, 2023

Manufacturers
FDA

Pella Pharmaceuticals Co. Ltd

DUNS: 562370925

Products 1

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

Erythromycin

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code82160-126
Product Classification
G
Generic Name
Erythromycin
Product Specifications
Route of AdministrationTOPICAL
Effective DateDecember 26, 2023
FDA Product Classification

INGREDIENTS (1)

ERYTHROMYCINActive
Quantity: 1200 mg in 30 g
Code: 63937KV33D
Classification: ACTIB

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Spotex - FDA Drug Approval Details