Drugplain

BETAMETHASONE DIPROPIONATE .5 mg/g

BETAMETHASONE DIPROPIONATE · OINTMENT, AUGMENTED · Aurobindo Pharma Limited

No Recall History
Plain English

BETAMETHASONE DIPROPIONATE is a ointment, augmented containing betamethasone dipropionate at .5 mg/g, taken topical. Manufactured by Aurobindo Pharma Limited.

Key Facts

Brand Name
BETAMETHASONE DIPROPIONATE
Generic Name
BETAMETHASONE DIPROPIONATE
NDC Code (Product)
59651-699
Manufacturer
Aurobindo Pharma Limited
Strength
.5 mg/g
Dosage Form
OINTMENT, AUGMENTED
Route
TOPICAL
Marketing Status
Application #
ANDA218289
Marketing Start
04/10/2024

Recall History

No Recall History

Side Effects Reported to FDA

FDA FAERS database · These are reported events, not confirmed side effects

drug ineffective1,421 reports
off label use588 reports
psoriasis556 reports
macular degeneration526 reports
nausea512 reports
pain464 reports
pruritus460 reports
fatigue423 reports
pain in extremity394 reports
condition aggravated387 reports

Frequently Asked Questions

What is BETAMETHASONE DIPROPIONATE used for?

BETAMETHASONE DIPROPIONATE contains BETAMETHASONE DIPROPIONATE. It is a ointment, augmented taken topical. Consult your doctor for specific uses.

Is BETAMETHASONE DIPROPIONATE a controlled substance?

BETAMETHASONE DIPROPIONATE is not classified as a controlled substance by the DEA.

What is the generic name for BETAMETHASONE DIPROPIONATE?

The generic name for BETAMETHASONE DIPROPIONATE is BETAMETHASONE DIPROPIONATE. There are 11 other brand versions of BETAMETHASONE DIPROPIONATE.

What is the NDC code for BETAMETHASONE DIPROPIONATE .5 mg/g?

The NDC (National Drug Code) for BETAMETHASONE DIPROPIONATE .5 mg/g is 59651-699, listed by Aurobindo Pharma Limited.

Product NDC

59651-699

Package NDC

59651-699-14

Other Betamethasone Brands

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

Data from openFDA · Public domain (CC0 1.0)