Prescription drug · ANDA
Clobetasol Propionate NDC 72162-1438
Clobetasol propionate .5 mg/g · Gel · Topical · Bryant Ranch Prepack
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 72162-1438-2 | 72162143802 | 1 TUBE in 1 CARTON (72162-1438-2) / 15 g in 1 TUBEMarketed from Aug 16, 2023 | |
| 72162-1438-3 | 72162143803 | 1 TUBE in 1 CARTON (72162-1438-3) / 30 g in 1 TUBEMarketed from Aug 16, 2023 | |
| 72162-1438-6 | 72162143806 | 1 TUBE in 1 CARTON (72162-1438-6) / 60 g in 1 TUBEMarketed from Aug 16, 2023 |
How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- Clobetasol Propionate
- Generic name (nonproprietary)
- clobetasol propionate
- Active ingredients
- Clobetasol propionate — .5 mg/g
- Dosage form
- Gel
- Route
- Topical
- Labeler
- Bryant Ranch Prepack
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 075027
- Marketing start
- Listing expires
- Other FDA classes
- Corticosteroid Hormone Receptor Agonists (Mechanism)
- Identifiers
- Product ID 72162-1438_beb3d6d1-d7c3-4726-93fc-54cb0aea1665SPL ID beb3d6d1-d7c3-4726-93fc-54cb0aea1665SPL set ID f0ca99cd-6c54-44f8-a9b3-432e93fc5d59RxCUI 861434UNII 779619577M
- Pharmacologic class
- Corticosteroid
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Topical products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N472162143802followed by a unit qualifier and the quantityPackage 72162-1438-02. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective .
Indications (excerpt from the label)
INDICATIONS AND USAGE Clobetasol Propionate Gel, 0.05% is a super-high potency corticosteroid formulation indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses. Treatment beyond 2 consecutive weeks is not recommended, and the total dosage should not exceed 50 g/week because of the potential for the drug to suppress the hypothalamic-pituitary-adrenal (HPA) axis. Use in pediatric patients under 12 years of age is not recommended.
Excerpt only. Read the full label for complete information.
Other NDCs under ANDA 075027
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Clobetasol Propionate | Clobetasol propionate .5 mg/g | GelTopical | Padagis Israel Pharmaceuticals Ltd | 45802-925 |
| Clobetasol Propionate | Clobetasol propionate .5 mg/g | GelTopical | Bryant Ranch Prepack | 63629-8637 |
| Clobetasol Propionate | Clobetasol propionate .5 mg/g | GelTopical | Bryant Ranch Prepack | 63629-8638 |
| Clobetasol Propionate | Clobetasol propionate .5 mg/g | GelTopical | Bryant Ranch Prepack | 63629-8639 |