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FDA Approval

Alcortin A

FDA-approved pharmaceutical product with comprehensive regulatory information, manufacturing details, and complete labeling documentation.

FDA Approval Summary

Company
Primus Pharmaceuticals
DUNS: 130834745
Effective Date
October 30, 2009
Labeling Type
HUMAN PRESCRIPTION DRUG LABEL
Aloe vera leaf(10 mg in 1 g)

Registrants1

Companies and organizations registered with the FDA for this drug approval, including their contact information and regulatory details.

Sonar Products, Inc

104283945

Manufacturing Establishments1

FDA-registered manufacturing facilities and establishments involved in the production, packaging, or distribution of this drug product.

Sonar Products, Inc

Primus Pharmaceuticals

Sonar Products, Inc

104283945

Products1

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

Alcortin A

Product Details

NDC Product Code
68040-705
Route of Administration
TOPICAL
Effective Date
October 30, 2009
Code: 3X7931PO74Class: ACTIBQuantity: 20 mg in 1 g
Code: ZY81Z83H0XClass: ACTIBQuantity: 10 mg in 1 g
Code: 63W7IE88K8Class: ACTIBQuantity: 10 mg in 1 g
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