Prescription drug · ANDA
Betamethasone valerate NDC 62332-708
Betamethasone valerate 1.2 mg/g · Aerosol, Foam · Topical · Alembic Pharmaceuticals Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 62332-708-31 | 62332070831 | 1 CAN in 1 CARTON (62332-708-31) / 100 g in 1 CANMarketed from Aug 22, 2024 | |
| 62332-708-50 | 62332070850 | 1 CAN in 1 CARTON (62332-708-50) / 50 g in 1 CANMarketed from Aug 22, 2024 |
How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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)
- Betamethasone valerate
- Generic name (nonproprietary)
- betamethasone valerate
- Active ingredients
- Betamethasone valerate — 1.2 mg/g
- Dosage form
- Aerosol, Foam
- Route
- Topical
- Labeler
- Alembic Pharmaceuticals Inc.
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 215832
- Marketing start
- Listing expires
- Other FDA classes
- Corticosteroid Hormone Receptor Agonists (Mechanism)
- Identifiers
- Product ID 62332-708_f9ac5a23-005f-457a-baf7-ceaf86302e7bSPL ID f9ac5a23-005f-457a-baf7-ceaf86302e7bSPL set ID 3b6fa573-de04-4626-a39a-dca39def6df2RxCUI 1244634UNII 9IFA5XM7R2UPC 0362332708505
- 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
N462332070831followed by a unit qualifier and the quantityPackage 62332-0708-31. 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 Betamethasone valerate foam, 0.12% is a medium potency topical corticosteroid indicated for relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses of the scalp.
Excerpt only. Read the full label for complete information.
Other NDCs under ANDA 215832
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 |
|---|---|---|---|---|
| Betamethasone valerate | Betamethasone valerate 1.2 mg/g | Aerosol, FoamTopical | Alembic Pharmaceuticals Limited | 46708-708 |