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Chateal EQ

Chateal EQ(Levonorgestrel and Ethinyl Estradiol Tablets USP, 0.15 mg/0.03 mg) Rx only

Approved
Approval ID

4c59652c-49a6-4eed-b557-9abd3ffac541

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Sep 2, 2023

Manufacturers
FDA

Afaxys Pharma, LLC

DUNS: 080508656

Products 1

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

Levonorgestrel and Ethinyl Estradiol

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code50102-230
Application NumberANDA206866
Product Classification
M
Marketing Category
C73584
G
Generic Name
Levonorgestrel and Ethinyl Estradiol
Product Specifications
Effective DateSeptember 1, 2023
FDA Product Classification

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Chateal EQ - FDA Drug Approval Details