What is NDC 63629-7833?

63629-7833 is the product NDC for Sildenafil, Sildenafil citrate 50 mg/1 tablet, film coated, listed with the FDA by Bryant Ranch Prepack. It has 8 package NDCs, shown above in 10- and 11-digit form.

Bryant Ranch Prepack, NDC labeler code 63629. 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.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Sildenafil NDC 63629-7833 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)63629-7833Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63629-7833Add 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 NDC	11-digit (billing)	Package
63629-7833-1	6362978330163629783301	30 TABLET, FILM COATED in 1 BOTTLE (63629-7833-1)Marketed from Nov 13, 2018
63629-7833-2	6362978330263629783302	10 TABLET, FILM COATED in 1 BOTTLE (63629-7833-2)Marketed from Jan 28, 2019
63629-7833-3	6362978330363629783303	15 TABLET, FILM COATED in 1 BOTTLE (63629-7833-3)Marketed from Sep 13, 2019
63629-7833-4	6362978330463629783304	90 TABLET, FILM COATED in 1 BOTTLE (63629-7833-4)Marketed from Aug 11, 2026
63629-7833-5	6362978330563629783305	60 TABLET, FILM COATED in 1 BOTTLE (63629-7833-5)Marketed from Aug 11, 2026
63629-7833-6	6362978330663629783306	20 TABLET, FILM COATED in 1 BOTTLE (63629-7833-6)Marketed from Aug 11, 2026
63629-7833-7	6362978330763629783307	7 TABLET, FILM COATED in 1 BOTTLE (63629-7833-7)Marketed from Aug 11, 2026
63629-7833-8	6362978330863629783308	40 TABLET, FILM COATED in 1 BOTTLE (63629-7833-8)Marketed from Aug 11, 2026

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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 — 50 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Bryant Ranch PrepackNDC labeler code 63629
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 202023
Marketing start: Jun 28, 2018
Listing expires: Dec 31, 2027
Other FDA classes: Phosphodiesterase 5 Inhibitors (Mechanism)
Identifiers: Product ID 63629-7833_fd77efe1-6233-489b-838c-aa3c9cf9d3f5SPL ID fd77efe1-6233-489b-838c-aa3c9cf9d3f5SPL set ID dfe4f616-b5de-458c-a97b-ab860e32320cRxCUI 312950UNII 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

N463629783301 followed by a unit qualifier and the quantity

Package 63629-7833-01. 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 Aug 11, 2026.

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.

Full label on DailyMed (opens in a new tab)

About NDC 63629-7833

What is NDC 63629-7833?: 63629-7833 is the product NDC for Sildenafil, Sildenafil citrate 50 mg/1 tablet, film coated, listed with the FDA by Bryant Ranch Prepack. It has 8 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?: Bryant Ranch Prepack, NDC labeler code 63629. 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
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Sildenafil	Sildenafil citrate 25 mg/1	Tablet, Film coatedOral	Jubilant Cadista Pharmaceuticals Inc.	59746-434	59746-0434-0359746-0434-0459746-0434-05+2 more
Sildenafil	Sildenafil citrate 50 mg/1	Tablet, Film coatedOral	Jubilant Cadista Pharmaceuticals Inc.	59746-435	59746-0435-0159746-0435-0359746-0435-04+3 more
Sildenafil	Sildenafil citrate 100 mg/1	Tablet, Film coatedOral	Jubilant Cadista Pharmaceuticals Inc.	59746-436	59746-0436-0159746-0436-0359746-0436-04+3 more
Sildenafil	Sildenafil citrate 20 mg/1	TabletOral	REMEDYREPACK INC.	70518-4596	70518-4596-00
Sildenafilsildenafil citrate	Sildenafil citrate 25 mg/1	FilmOral	Yaral Pharma Inc.	82347-0205	82347-0205-0482347-0205-0582347-0205-06
Sildenafilsildenafil citrate	Sildenafil citrate 50 mg/1	FilmOral	Yaral Pharma Inc.	82347-0210	82347-0210-0482347-0210-0582347-0210-06
Sildenafilsildenafil citrate	Sildenafil citrate 75 mg/1	FilmOral	Yaral Pharma Inc.	82347-0215	82347-0215-0482347-0215-0582347-0215-06
Sildenafilsildenafil citrate	Sildenafil citrate 100 mg/1	FilmOral	Yaral Pharma Inc.	82347-0220	82347-0220-0482347-0220-0582347-0220-06
Sildenafil	Sildenafil citrate 20 mg/1	Tablet, Film coatedOral	Golden State Medical Supply, Inc.	51407-987	51407-0987-90
Sildenafil	Sildenafil citrate 20 mg/1	TabletOral	AvKARE	42291-937	42291-0937-90

All 151 Sildenafil NDCs

Other NDCs under ANDA 202023

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

FDA NDC Directory listings under ANDA 202023
Product	Strength	Form · route	Labeler	Product NDC
Sildenafil	Sildenafil citrate 25 mg/1	Tablet, Film coatedOral	Amneal Pharmaceuticals NY LLC	60219-1751
Sildenafil	Sildenafil citrate 50 mg/1	Tablet, Film coatedOral	Amneal Pharmaceuticals NY LLC	60219-1752
Sildenafil	Sildenafil citrate 100 mg/1	Tablet, Film coatedOral	Amneal Pharmaceuticals NY LLC	60219-1753
Sildenafil	Sildenafil citrate 100 mg/1	Tablet, Film coatedOral	NuCare Pharmaceuticals,Inc.	68071-2985
Sildenafil	Sildenafil citrate 100 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	71335-0969