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FDA Drug information

CLOBETASOL PROPIONATE

Read time: 1 mins
Marketing start date: 28 Apr 2024
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Summary of product characteristics


Effective Time

20220804

Version

5

Spl Product Data Elements

CLOBETASOL PROPIONATE CLOBETASOL PROPIONATE CLOBETASOL PROPIONATE CLOBETASOL PROPYLENE GLYCOL SORBITAN SESQUIOLEATE PETROLATUM

Application Number

ANDA210199

Brand Name

CLOBETASOL PROPIONATE

Generic Name

CLOBETASOL PROPIONATE

Product Ndc

70771-1209

Product Type

HUMAN PRESCRIPTION DRUG

Route

TOPICAL

Package Label Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL NDC 70771-1209-1 Clobetasol Propionate Ointment USP, 0.05% Rx only 15 g clobetasole ointment label

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Disclaimer

The drug Prescribing Information (PI), including indications, contra-indications, interactions, etc, has been developed using the U.S. Food & Drug Administration (FDA) as a source (www.fda.gov).

Medthority offers the whole library of PI documents from the FDA. Medthority will not be held liable for explicit or implicit errors, or missing data.

Drugs appearing in this section are approved by the FDA. For regions outside of the United States, this content is for informational purposes only and may not be aligned with local regulatory approvals or guidance.