Prescription drug · ANDA
Betamethasone Dipropionate NDC 51672-1274
Betamethasone dipropionate .5 mg/g · Cream · Topical · Sun Pharmaceutical Industries, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 51672-1274-1 | 5167212740151672127401 | 1 TUBE in 1 CARTON (51672-1274-1) / 15 g in 1 TUBEMarketed from Apr 30, 1992 | |
| 51672-1274-6 | 5167212740651672127406 | 1 TUBE in 1 CARTON (51672-1274-6) / 45 g in 1 TUBEMarketed from Apr 30, 1992 |
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)
- Betamethasone Dipropionate
- Generic name (nonproprietary)
- betamethasone dipropionate
- Active ingredients
- Betamethasone dipropionate — .5 mg/g
- Dosage form
- Cream
- Route
- Topical
- Labeler
- Sun Pharmaceutical Industries, Inc.NDC labeler code 51672
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 073552
- Marketing start
- Listing expires
- Other FDA classes
- Corticosteroid Hormone Receptor Agonists (Mechanism)
- Identifiers
- Product ID 51672-1274_38f55e1e-dffd-ee76-e063-6394a90aee5eSPL ID 38f55e1e-dffd-ee76-e063-6394a90aee5eSPL set ID bc12c828-54ba-411d-b752-9b735f7adf63RxCUI 238920UNII 826Y60901U
- 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
N451672127401followed by a unit qualifier and the quantityPackage 51672-1274-01. 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 dipropionate cream is a medium-potency corticosteroid indicated for relief of the inflammatory and pruritic manifestations of corticosteroid responsive dermatoses in patients 13 years and older.
Excerpt only. Read the full label for complete information.
About NDC 51672-1274
- What is NDC 51672-1274?
- 51672-1274 is the product NDC for Betamethasone Dipropionate, Betamethasone dipropionate .5 mg/g cream, listed with the FDA by Sun Pharmaceutical Industries, Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Betamethasone Dipropionate.
- What is the active ingredient?
- Betamethasone dipropionate.
- Who is the labeler?
- Sun Pharmaceutical Industries, Inc., NDC labeler code 51672. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Betamethasone Dipropionate?
- 53 other product NDCs are listed under this name. See all Betamethasone Dipropionate NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Betamethasone Dipropionate products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Betamethasone Dipropionate | Betamethasone dipropionate .5 mg/g | CreamTopical | Aurobindo Pharma Limited | 59651-891 | 59651-0891-1459651-0891-46 |
| Betamethasone Dipropionate | Betamethasone dipropionate .5 mg/mL | Lotion, AugmentedTopical | Encube Ethicals, Inc. | 21922-104 | 21922-0104-0121922-0104-21 |
| Betamethasone Dipropionate | Betamethasone dipropionate .5 mg/g | Ointment, AugmentedTopical | Burel Pharmaceuticals, LLC | 35573-107 | 35573-0107-1535573-0107-49 |
| Betamethasone Dipropionate | Betamethasone dipropionate .5 mg/g | CreamTopical | REMEDYREPACK INC. | 70518-4187 | 70518-4187-00 |
| Betamethasone Dipropionate | Betamethasone dipropionate .5 mg/g | Ointment, AugmentedTopical | Aurobindo Pharma Limited | 59651-699 | 59651-0699-1459651-0699-4659651-0699-50 |
| Betamethasone Dipropionate | Betamethasone dipropionate .5 mg/g | OintmentTopical | Bryant Ranch Prepack | 63629-9323 | 63629-9323-01 |
| Betamethasone Dipropionate | Betamethasone dipropionate .5 mg/g | OintmentTopical | Bryant Ranch Prepack | 63629-9324 | 63629-9324-01 |
| Betamethasone Dipropionate | Betamethasone dipropionate .5 mg/g | OintmentTopical | Padagis Israel Pharmaceuticals Ltd | 45802-505 | 45802-0505-1445802-0505-84 |
| Betamethasone Dipropionate | Betamethasone dipropionate .5 mg/g | OintmentTopical | Bryant Ranch Prepack | 71335-2715 | 71335-2715-01 |
| Betamethasone Dipropionate | Betamethasone dipropionate .5 mg/g | OintmentTopical | Bryant Ranch Prepack | 72162-1415 | 72162-1415-0272162-1415-04 |
Other NDCs under ANDA 073552
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 Dipropionate | Betamethasone dipropionate .5 mg/g | CreamTopical | A-S Medication Solutions | 50090-3276 |
| Betamethasone Dipropionate | Betamethasone dipropionate .5 mg/g | CreamTopical | Golden State Medical Supply, Inc. | 51407-273 |