What is NDC 31722-100?

31722-100 is the product NDC for Nitazoxanide, Nitazoxanide 500 mg/1 tablet, film coated, listed with the FDA by Camber Pharmaceuticals, Inc.. It has 3 package NDCs, shown above in 10- and 11-digit form.

Camber Pharmaceuticals, Inc., NDC labeler code 31722. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Nitazoxanide?

3 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Nitazoxanide NDC 31722-100 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)31722-100Labeler and product segments. Claims need a package NDC.

Product NDC at billing width31722-0100Add 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
31722-100-30	31722010030	1 BOTTLE in 1 CARTON (31722-100-30) / 30 TABLET, FILM COATED in 1 BOTTLEMarketed from Apr 15, 2025
31722-100-31	31722010031	1 BOTTLE in 1 CARTON (31722-100-31) / 12 TABLET, FILM COATED in 1 BOTTLEMarketed from Apr 15, 2025
31722-100-32	31722010032	1 BOTTLE in 1 CARTON (31722-100-32) / 6 TABLET, FILM COATED in 1 BOTTLEMarketed from Apr 15, 2025

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): Nitazoxanide
Generic name (nonproprietary): nitazoxanide
Active ingredients: Nitazoxanide — 500 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Camber Pharmaceuticals, Inc.NDC labeler code 31722
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 218701
Marketing start: Apr 15, 2025
Listing expires: Dec 31, 2026
Identifiers: Product ID 31722-100_4729e7ee-3333-ee2b-e063-6394a90aa85cSPL ID 4729e7ee-3333-ee2b-e063-6394a90aa85cSPL set ID 295011e1-f919-4e5a-b9e7-4c784f623a86RxCUI 427163UNII SOA12P041NUPC 0331722100311
Pharmacologic class: Antiprotozoal

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

N431722010030 followed by a unit qualifier and the quantity

Package 31722-0100-30. 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 Dec 30, 2025.

Indications (excerpt from the label)

Diarrhea caused by Giardia lamblia or Cryptosporidium parvum: Nitazoxanide tablets (patients 12 years and older) are indicated for the treatment of diarrhea caused by Giardia lamblia or Cryptosporidium parvum . Limitations of Use Nitazoxanide tablets have not been shown to be effective for the treatment of diarrhea caused by Cryptosporidium parvum in HIV-infected or immunodeficient patients [see Clinical Studies (14.2) ] . Nitazoxanide tablets are antiprotozoal indicated for the treatment of diarrhea caused by Giardia lamblia or Cryptosporidium parvum (1 ). Limitations of Use: Nitazoxanide tablets have not been shown to be effective for the treatment of diarrhea caused by C. parvum in HIV-in…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 31722-100

What is NDC 31722-100?: 31722-100 is the product NDC for Nitazoxanide, Nitazoxanide 500 mg/1 tablet, film coated, listed with the FDA by Camber Pharmaceuticals, Inc.. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Nitazoxanide.
What is the active ingredient?: Nitazoxanide.
Who is the labeler?: Camber Pharmaceuticals, Inc., NDC labeler code 31722. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Nitazoxanide?: 3 other product NDCs are listed under this name. See all Nitazoxanide 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 Nitazoxanide NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Nitazoxanide	Nitazoxanide 500 mg/1	TabletOral	e5 Pharma, LLC	13517-135	13517-0135-06
Nitazoxanide	Nitazoxanide 500 mg/1	TabletOral	ANI Pharmaceuticals, Inc.	70954-934	70954-0934-10
Nitazoxanide	Nitazoxanide 500 mg/1	Tablet, Film coatedOral	Rising Pharma Holdings, Inc.	64980-526	64980-0526-0364980-0526-2164980-0526-60+1 more