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OCELLA

OCELLA 28 TABLETS(drospirenone and ethinyl estradiol)

Approved
Approval ID

4fedeb6a-d99f-43e1-89f3-75818ce919aa

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Feb 23, 2011

Manufacturers
FDA

Physicians Total Care, Inc.

DUNS: 194123980

Products 1

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

drospirenone and ethinyl estradiol

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code54868-5922
Application NumberNDA021098
Product Classification
M
Marketing Category
C73594
G
Generic Name
drospirenone and ethinyl estradiol
Product Specifications
Effective DateJune 13, 2011
FDA Product Classification

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OCELLA - FDA Drug Approval Details