Cefprozil NDC 57237-036

NDC codes

FDA NDC Directory

Product NDC (as listed)57237-036Labeler and product segments. Claims need a package NDC.

Product NDC at billing width57237-0036Add 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	Copy
57237-036-01	57237003601	100 TABLET, FILM COATED in 1 BOTTLE (57237-036-01)Marketed from May 24, 2007

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): Cefprozil
Generic name (nonproprietary): cefprozil
Active ingredients: Cefprozil — 250 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Rising Pharma Holdings, Inc.
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 065340
Marketing start: May 24, 2007
Listing expires: Dec 31, 2026
Identifiers: Product ID 57237-036_ccfc6236-d155-4a97-8cbf-a5d4592e677fSPL ID ccfc6236-d155-4a97-8cbf-a5d4592e677fSPL set ID af24a86f-8072-49a6-94ec-2f17fe81812bRxCUI 197452, 197453UNII 4W0459ZA4VUPC 0357237036013, 0357237037010

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

N457237003601 followed by a unit qualifier and the quantity

Package 57237-0036-01. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 065340

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

FDA NDC Directory listings under ANDA 065340
Product	Strength	Form · route	Labeler	Product NDC
Cefprozil	Cefprozil 500 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-1710
Cefprozil	Cefprozil 500 mg/1	Tablet, Film coatedOral	Rising Pharma Holdings, Inc.	57237-037
Cefprozil	Cefprozil 250 mg/1	Tablet, Film coatedOral	NorthStar Rx LLC	16714-398
Cefprozil	Cefprozil 500 mg/1	Tablet, Film coatedOral	NorthStar Rx LLC	16714-399
Cefprozil	Cefprozil 250 mg/1	Tablet, Film coatedOral	Aurobindo Pharma Limited	65862-068
Cefprozil	Cefprozil 500 mg/1	Tablet, Film coatedOral	Aurobindo Pharma Limited	65862-069