NDC codes

FDA NDC Directory
Product NDC (as listed)82647-210Labeler and product segments. Claims need a package NDC.
Product NDC at billing width82647-0210Add 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
82647-210-1482647021014826470210141000 TABLET, FILM COATED in 1 BOTTLE (82647-210-14)Marketed from Mar 28, 2022
82647-210-30826470210308264702103030 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 CorporationNDC labeler code 82647
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

N482647021014 followed by a unit qualifier and the quantity

Package 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.

Full label on DailyMed (opens in a new tab)

About NDC 82647-210

What is NDC 82647-210?
82647-210 is the product NDC for Sildenafil, Sildenafil citrate 25 mg/1 tablet, film coated, listed with the FDA by Reyoung Corporation. It has 2 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?
Reyoung Corporation, NDC labeler code 82647. 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 208494

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

FDA NDC Directory listings under ANDA 208494
ProductStrengthForm · routeLabelerProduct NDC
SildenafilSildenafil citrate 25 mg/1Tablet, Film coatedOralBostal LLC35561-251
SildenafilSildenafil citrate 50 mg/1Tablet, Film coatedOralBostal LLC35561-252
SildenafilSildenafil citrate 100 mg/1Tablet, Film coatedOralBostal LLC35561-253
SildenafilSildenafil citrate 50 mg/1Tablet, Film coatedOralReyoung Corporation82647-211
SildenafilSildenafil citrate 100 mg/1Tablet, Film coatedOralReyoung Corporation82647-212

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