NDC codes

FDA NDC Directory
Product NDC (as listed)71205-473Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71205-0473Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
71205-473-10712050473107120504731010 TABLET in 1 BOTTLE (71205-473-10)Marketed from Aug 24, 2020
71205-473-20712050473207120504732020 TABLET in 1 BOTTLE (71205-473-20)Marketed from Mar 23, 2021
71205-473-30712050473307120504733030 TABLET in 1 BOTTLE (71205-473-30)Marketed from Aug 24, 2020
71205-473-60712050473607120504736060 TABLET in 1 BOTTLE (71205-473-60)Marketed from Aug 24, 2020
71205-473-90712050473907120504739090 TABLET in 1 BOTTLE (71205-473-90)Marketed from Aug 24, 2020

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
Route
Oral
Labeler
Proficient Rx LPNDC labeler code 71205
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 207178
Marketing start
Listing expires
Other FDA classes
Phosphodiesterase 5 Inhibitors (Mechanism)
Identifiers
Product ID 71205-473_1d2a3b34-3e71-4a4b-81ed-4ff35976abc0SPL ID 1d2a3b34-3e71-4a4b-81ed-4ff35976abc0SPL set ID 7086e222-0f2b-4c02-84c0-4f8635c90993RxCUI 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

N471205047310 followed by a unit qualifier and the quantity

Package 71205-0473-10. 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 is a phosphodiesterase-5 (PDE5) inhibitor indicated for the treatment of erectile dysfunction (ED)

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71205-473

What is NDC 71205-473?
71205-473 is the product NDC for Sildenafil, Sildenafil citrate 100 mg/1 tablet, listed with the FDA by Proficient Rx LP. It has 5 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Sildenafil.
What is the active ingredient?
Sildenafil citrate.
Who is the labeler?
Proficient Rx LP, NDC labeler code 71205. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Sildenafil?
150 other product NDCs are listed under this name. See all Sildenafil NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Sildenafil NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
SildenafilSildenafil citrate 25 mg/1Tablet, Film coatedOralJubilant Cadista Pharmaceuticals Inc.59746-43459746-0434-0359746-0434-0459746-0434-05+2 more
SildenafilSildenafil citrate 50 mg/1Tablet, Film coatedOralJubilant Cadista Pharmaceuticals Inc.59746-43559746-0435-0159746-0435-0359746-0435-04+3 more
SildenafilSildenafil citrate 100 mg/1Tablet, Film coatedOralJubilant Cadista Pharmaceuticals Inc.59746-43659746-0436-0159746-0436-0359746-0436-04+3 more
SildenafilSildenafil citrate 20 mg/1TabletOralREMEDYREPACK INC.70518-459670518-4596-00
Sildenafilsildenafil citrateSildenafil citrate 25 mg/1FilmOralYaral Pharma Inc.82347-020582347-0205-0482347-0205-0582347-0205-06
Sildenafilsildenafil citrateSildenafil citrate 50 mg/1FilmOralYaral Pharma Inc.82347-021082347-0210-0482347-0210-0582347-0210-06
Sildenafilsildenafil citrateSildenafil citrate 75 mg/1FilmOralYaral Pharma Inc.82347-021582347-0215-0482347-0215-0582347-0215-06
Sildenafilsildenafil citrateSildenafil citrate 100 mg/1FilmOralYaral Pharma Inc.82347-022082347-0220-0482347-0220-0582347-0220-06
SildenafilSildenafil citrate 20 mg/1Tablet, Film coatedOralGolden State Medical Supply, Inc.51407-98751407-0987-90
SildenafilSildenafil citrate 20 mg/1TabletOralAvKARE42291-93742291-0937-90

All 151 Sildenafil NDCs

Other NDCs under ANDA 207178

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 207178
ProductStrengthForm · routeLabelerProduct NDC
SildenafilSildenafil citrate 25 mg/1TabletOralAppco Pharma LLC55801-338
SildenafilSildenafil citrate 50 mg/1TabletOralAppco Pharma LLC55801-339
SildenafilSildenafil citrate 100 mg/1TabletOralAppco Pharma LLC55801-340
SildenafilSildenafil citrate 25 mg/1TabletOralCIPLA USA INC.,69097-951
SildenafilSildenafil citrate 50 mg/1TabletOralCIPLA USA INC.,69097-952
SildenafilSildenafil citrate 100 mg/1TabletOralCIPLA USA INC.,69097-953
SildenafilSildenafil citrate 100 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-675
SildenafilSildenafil citrate 50 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-679
SildenafilSildenafil citrate 25 mg/1TabletOralExelan Pharmaceuticals, Inc.76282-643
SildenafilSildenafil citrate 50 mg/1TabletOralExelan Pharmaceuticals, Inc.76282-644
SildenafilSildenafil citrate 100 mg/1TabletOralExelan Pharmaceuticals, Inc.76282-645

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