United States · FDA National Drug Code directory

Betamethasone Dipropionate

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
0713-0807_ed81406a-8c03-5c33-e053-2a95a90a941f
Product NDC
0713-0807
Form
LOTION
Composition / generic term
Betamethasone Dipropionate
Labeler
Cosette Pharmaceuticals, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20160905
Source listing expiry
20261231

Source-listed ingredients

  • BETAMETHASONE DIPROPIONATE — .5 mg/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BOTTLE in 1 CARTON (0713-0807-53) / 60 mL in 1 BOTTLE · 0713-0807-53

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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Betamethasone Dipropionate — United States | Molindra Medicines