Prescription drug · ANDA
Diflorasone Diacetate NDC 51672-1295
Diflorasone diacetate .5 mg/g · Ointment · Topical · Sun Pharmaceutical Industries, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 51672-1295-1 | 5167212950151672129501 | 1 TUBE in 1 CARTON (51672-1295-1) / 15 g in 1 TUBEMarketed from May 14, 1999 | |
| 51672-1295-2 | 5167212950251672129502 | 1 TUBE in 1 CARTON (51672-1295-2) / 30 g in 1 TUBEMarketed from May 14, 1999 | |
| 51672-1295-3 | 5167212950351672129503 | 1 TUBE in 1 CARTON (51672-1295-3) / 60 g in 1 TUBEMarketed from May 14, 1999 |
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)
- Diflorasone Diacetate
- Generic name (nonproprietary)
- diflorasone diacetate
- Active ingredients
- Diflorasone diacetate — .5 mg/g
- Dosage form
- Ointment
- 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 075331
- Marketing start
- Listing expires
- Other FDA classes
- Corticosteroid Hormone Receptor Agonists (Mechanism)
- Identifiers
- Product ID 51672-1295_39095d21-70bb-6f1d-e063-6394a90a9b9dSPL ID 39095d21-70bb-6f1d-e063-6394a90a9b9dSPL set ID b304dfca-e840-4c03-8217-73aaa5360277RxCUI 966607UNII 7W2J09SCWX
- 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
N451672129501followed by a unit qualifier and the quantityPackage 51672-1295-01. 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 Topical corticosteroids are indicated for relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses.
Excerpt only. Read the full label for complete information.
About NDC 51672-1295
- What is NDC 51672-1295?
- 51672-1295 is the product NDC for Diflorasone Diacetate, Diflorasone diacetate .5 mg/g ointment, listed with the FDA by Sun Pharmaceutical Industries, Inc.. It has 3 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Diflorasone Diacetate.
- What is the active ingredient?
- Diflorasone diacetate.
- 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 Diflorasone Diacetate?
- 2 other product NDCs are listed under this name. See all Diflorasone Diacetate NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Diflorasone Diacetate products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Diflorasone Diacetate | Diflorasone diacetate .5 mg/g | OintmentTopical | Rising Pharma Holdings, Inc. | 64980-124 | 64980-0124-0364980-0124-1564980-0124-45+1 more |
| Diflorasone Diacetate | Diflorasone diacetate .5 mg/g | CreamTopical | Sun Pharmaceutical Industries, Inc. | 51672-1296 | 51672-1296-0151672-1296-0251672-1296-03 |