Prescription drug · ANDA
Roflumilast NDC 0904-7483
Roflumilast 500 ug/1 · Tablet · Oral · Major Pharmaceuticals
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 0904-7483-03 | 00904748303 | 30 TABLET in 1 BOTTLE (0904-7483-03)Marketed from May 22, 2024 | |
| 0904-7483-89 | 00904748389 | 90 TABLET in 1 BOTTLE (0904-7483-89)Marketed from May 22, 2024 |
How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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)
- Roflumilast
- Generic name (nonproprietary)
- roflumilast
- Active ingredients
- Roflumilast — 500 ug/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- Major Pharmaceuticals
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 208256
- Marketing start
- Listing expires
- Other FDA classes
- Phosphodiesterase 4 Inhibitors (Mechanism)
- Identifiers
- Product ID 0904-7483_afaf51f3-1276-4631-b549-ceb1a21aa925SPL ID afaf51f3-1276-4631-b549-ceb1a21aa925SPL set ID ca22f3e0-6f33-4f1c-97e5-0c962891067aRxCUI 1091839UNII 0P6C6ZOP5U
- Pharmacologic class
- Phosphodiesterase 4 Inhibitor
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. Oral products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N400904748303followed by a unit qualifier and the quantityPackage 00904-7483-03. 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)
Roflumilast Tablets are indicated as a treatment to reduce the risk of COPD exacerbations in patients with severe COPD associated with chronic bronchitis and a history of exacerbations. Limitations of Use Roflumilast Tablets are not a bronchodilator and is not indicated for the relief of acute bronchospasm. Roflumilast Tablets 250 mcg is a starting dose, for the first 4 weeks of treatment only and is not the effective (therapeutic) dose. Roflumilast Tablets are a selective phosphodiesterase 4 inhibitor indicated as a treatment to reduce the risk of COPD exacerbations in patients with severe COPD associated with chronic bronchitis and a history of exacerbations. ( 1 , 14 ) Limitations of Use:…
Excerpt only. Read the full label for complete information.
Other NDCs under ANDA 208256
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 |
|---|---|---|---|---|
| Roflumilast | Roflumilast 250 ug/1 | TabletOral | MAJOR PHARMACEUTICALS | 0904-7493 |
| Roflumilast | Roflumilast 500 ug/1 | TabletOral | Novadoz Pharmaceuticals LLC | 72205-200 |
| Roflumilast | Roflumilast 250 ug/1 | TabletOral | Novadoz Pharmaceuticals LLC | 72205-201 |
| Roflumilast | Roflumilast 500 ug/1 | TabletOral | MAJOR PHARMACEUTICALS | 0904-7399 |