Prescription drug · ANDA
Sildenafil NDC 82647-210
Sildenafil citrate 25 mg/1 · Tablet, Film coated · Oral · Reyoung Corporation
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 82647-210-14 | 82647021014 | 1000 TABLET, FILM COATED in 1 BOTTLE (82647-210-14)Marketed from Mar 28, 2022 | |
| 82647-210-30 | 82647021030 | 30 TABLET, FILM COATED in 1 BOTTLE (82647-210-30)Marketed from Mar 28, 2022 |
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)
- Sildenafil
- Generic name (nonproprietary)
- sildenafil
- Active ingredients
- Sildenafil citrate — 25 mg/1
- Dosage form
- Tablet, Film coated
- Route
- Oral
- Labeler
- Reyoung Corporation
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 208494
- Marketing start
- Listing expires
- Other FDA classes
- Phosphodiesterase 5 Inhibitors (Mechanism)
- Identifiers
- Product ID 82647-210_49fd0cc5-980e-c7d1-e063-6394a90a85c0SPL ID 49fd0cc5-980e-c7d1-e063-6394a90a85c0SPL set ID dc998a9c-0770-111b-e053-2a95a90a88a4RxCUI 312950, 314228, 314229UNII BW9B0ZE037UPC 0382647211149, 0382647210142
- Pharmacologic class
- Phosphodiesterase 5 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
N482647021014followed by a unit qualifier and the quantityPackage 82647-0210-14. 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)
SILDENAFIL TABLETS is indicated for the treatment of erectile dysfunction. SILDENAFIL TABLETS is a phosphodiesterase-5 (PDE5) inhibitor indicated for the treatment of erectile dysfunction (ED) (1)
Excerpt only. Read the full label for complete information.
Other NDCs under ANDA 208494
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 |
|---|---|---|---|---|
| Sildenafil | Sildenafil citrate 50 mg/1 | Tablet, Film coatedOral | Reyoung Corporation | 82647-211 |
| Sildenafil | Sildenafil citrate 100 mg/1 | Tablet, Film coatedOral | Reyoung Corporation | 82647-212 |
| Sildenafil | Sildenafil citrate 25 mg/1 | Tablet, Film coatedOral | Bostal LLC | 35561-251 |
| Sildenafil | Sildenafil citrate 50 mg/1 | Tablet, Film coatedOral | Bostal LLC | 35561-252 |
| Sildenafil | Sildenafil citrate 100 mg/1 | Tablet, Film coatedOral | Bostal LLC | 35561-253 |