Prescription drug · ANDA
Sildenafil NDC 71205-088
Sildenafil citrate 100 mg/1 · Tablet, Film coated · Oral · Proficient Rx LP
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 71205-088-10 | 71205008810 | 10 TABLET, FILM COATED in 1 BOTTLE (71205-088-10)Marketed from Aug 1, 2018 | |
| 71205-088-20 | 71205008820 | 20 TABLET, FILM COATED in 1 BOTTLE (71205-088-20)Marketed from Apr 21, 2021 | |
| 71205-088-30 | 71205008830 | 30 TABLET, FILM COATED in 1 BOTTLE (71205-088-30)Marketed from Aug 1, 2018 | |
| 71205-088-50 | 71205008850 | 50 TABLET, FILM COATED in 1 BOTTLE (71205-088-50)Marketed from Aug 1, 2018 | |
| 71205-088-60 | 71205008860 | 60 TABLET, FILM COATED in 1 BOTTLE (71205-088-60)Marketed from Aug 1, 2018 | |
| 71205-088-90 | 71205008890 | 90 TABLET, FILM COATED in 1 BOTTLE (71205-088-90)Marketed from Aug 1, 2018 |
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 — 100 mg/1
- Dosage form
- Tablet, Film coated
- Route
- Oral
- Labeler
- Proficient Rx LP
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 077342
- Marketing start
- Listing expires
- Other FDA classes
- Phosphodiesterase 5 Inhibitors (Mechanism)
- Identifiers
- Product ID 71205-088_ebc2e212-b59d-464c-a0cd-ede59263c5daSPL ID ebc2e212-b59d-464c-a0cd-ede59263c5daSPL set ID 43a036a4-8a34-4411-ac8e-bf5063d67d48RxCUI 314229UNII BW9B0ZE037
- 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
N471205008810followed by a unit qualifier and the quantityPackage 71205-0088-10. 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 are indicated for the treatment of erectile dysfunction. Sildenafil tablets are 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 077342
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 | Proficient Rx LP | 71205-267 |
| Sildenafil | Sildenafil citrate 100 mg/1 | Tablet, Film coatedOral | Bryant Ranch Prepack | 71335-1777 |
| Sildenafil | Sildenafil citrate 25 mg/1 | Tablet, Film coatedOral | Teva Pharmaceuticals USA, Inc. | 0093-5341 |
| Sildenafil | Sildenafil citrate 50 mg/1 | Tablet, Film coatedOral | Teva Pharmaceuticals USA, Inc. | 0093-5342 |
| Sildenafil | Sildenafil citrate 100 mg/1 | Tablet, Film coatedOral | Teva Pharmaceuticals USA, Inc. | 0093-5343 |