Cefdinir NDC 0093-4137

NDC codes

FDA NDC Directory

Product NDC (as listed)0093-4137Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00093-4137Add 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
0093-4137-64	00093413764	60 mL in 1 BOTTLE (0093-4137-64)Marketed from May 8, 2007
0093-4137-73	00093413773	100 mL in 1 BOTTLE (0093-4137-73)Marketed from May 8, 2007

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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): Cefdinir
Generic name (nonproprietary): cefdinir
Active ingredients: Cefdinir monohydrate — 250 mg/5mL
Dosage form: Powder, For suspension
Route: Oral
Labeler: Teva Pharmaceuticals USA, Inc.
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 065332
Marketing start: May 8, 2007
Listing expires: Dec 31, 2026
Other FDA classes: Cephalosporins (Chemical structure)
Identifiers: Product ID 0093-4137_7f269e55-b085-4315-807a-e425f0189b2cSPL ID 7f269e55-b085-4315-807a-e425f0189b2cSPL set ID a1f49fe1-b511-4f6b-a912-8ae8662d95a5RxCUI 309054, 476576UNII 6E7SN358SE
Pharmacologic class: Cephalosporin Antibacterial

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

N400093413764 followed by a unit qualifier and the quantity

Package 00093-4137-64. 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 065332

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

FDA NDC Directory listings under ANDA 065332
Product	Strength	Form · route	Labeler	Product NDC
Cefdinir	Cefdinir 125 mg/5mL	Powder, For suspensionOral	A-S Medication Solutions	50090-4258
Cefdinir	Cefdinir monohydrate 250 mg/5mL	Powder, For suspensionOral	Proficient Rx LP	63187-616
Cefdinir	Cefdinir monohydrate 125 mg/5mL	Powder, For suspensionOral	NuCare Pharmaceuticals, Inc.	68071-3156
Cefdinir	Cefdinir monohydrate 250 mg/5mL	Powder, For suspensionOral	Preferred Pharmaceuticals Inc.	68788-8655
Cefdinir	Cefdinir monohydrate 250 mg/5mL	Powder, For suspensionOral	A-S Medication Solutions	50090-3725
Cefdinir	Cefdinir monohydrate 125 mg/5mL	Powder, For suspensionOral	Teva Pharmaceuticals USA, Inc.	0093-4136