Drugplain

Betamethasone Dipropionate USP, 0.05% .5 mg/g

Betamethasone Dipropionate USP, 0.05% · OINTMENT · TruPharma LLC

No Recall History
Plain English

Betamethasone Dipropionate USP, 0.05% is a ointment containing betamethasone dipropionate usp, 0.05% at .5 mg/g, taken topical. Manufactured by TruPharma LLC.

Key Facts

Brand Name
Betamethasone Dipropionate USP, 0.05%
Generic Name
Betamethasone Dipropionate USP, 0.05%
NDC Code (Product)
52817-824
Manufacturer
TruPharma LLC
Strength
.5 mg/g
Dosage Form
OINTMENT
Route
TOPICAL
Marketing Status
Application #
ANDA215186
Marketing Start
02/18/2022

Recall History

No Recall History

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

INDICATIONS AND USAGE Topical corticosteroids are indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses.

Dosage & Administration

DOSAGE AND ADMINISTRATION Apply a thin film of betamethasone dipropionate ointment to the affected skin areas once daily. In some cases, twice daily dosage may be necessary. If an infection develops, appropriate antimicrobial therapy should be instituted. Betamethasone dipropionate ointment should not be used with occlusive dressings.

Contraindications

CONTRAINDICATIONS Topical corticosteroids are contraindicated in those patients with a history of hypersensitivity to any of the components of the preparation.

Adverse Reactions

ADVERSE REACTIONS The following local adverse reactions are reported infrequently when betamethasone dipropionate ointment is used as recommended in the DOSAGE AND ADMINISTRATION section. These reactions are listed in an approximate decreasing order of occurrence: burning, itching, irritation, dryness, folliculitis, hypertrichosis, acneiform eruptions, hypopigmentation, perioral dermatitis, allergic contact dermatitis, maceration of the skin, secondary infections, skin atrophy, striae and miliaria. Systemic absorption of topical corticosteroids has produced reversible hypothalamic-pituitary-adrenal (HPA) axis suppression, manifestations of Cushing's syndrome, hyperglycemia and glucosuria in some patients.

Frequently Asked Questions

What is Betamethasone Dipropionate USP, 0.05% used for?

Betamethasone Dipropionate USP, 0.05% contains Betamethasone Dipropionate USP, 0.05%. It is a ointment taken topical. Consult your doctor for specific uses.

Is Betamethasone Dipropionate USP, 0.05% a controlled substance?

Betamethasone Dipropionate USP, 0.05% is not classified as a controlled substance by the DEA.

What is the generic name for Betamethasone Dipropionate USP, 0.05%?

The generic name for Betamethasone Dipropionate USP, 0.05% is Betamethasone Dipropionate USP, 0.05%. There are no other listed brand versions of Betamethasone Dipropionate USP, 0.05%.

What is the NDC code for Betamethasone Dipropionate USP, 0.05% .5 mg/g?

The NDC (National Drug Code) for Betamethasone Dipropionate USP, 0.05% .5 mg/g is 52817-824, listed by TruPharma LLC.

Product NDC

52817-824

Package NDC

52817-824-15

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)