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
- 45802-505_46112f27-facd-420e-9de1-289de334cbf9
- Product NDC
- 45802-505
- Form
- OINTMENT
- Composition / generic term
- betamethasone dipropionate
- Labeler
- Padagis Israel Pharmaceuticals Ltd
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220520
- Source listing expiry
- 20261231
Source-listed ingredients
- BETAMETHASONE DIPROPIONATE — .5 mg/g
These values do not establish equivalence or a dose recommendation.
Packages
- 1 TUBE in 1 CARTON (45802-505-14) / 15 g in 1 TUBE · 45802-505-14
- 1 TUBE in 1 CARTON (45802-505-84) / 45 g in 1 TUBE · 45802-505-84
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.
Browse United States records →