NDC codes

FDA NDC Directory
Product NDC (as listed)72578-007Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72578-0007Add 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
72578-007-0172578000701100 TABLET in 1 BOTTLE (72578-007-01)Marketed from Feb 23, 2019
72578-007-0572578000705500 TABLET in 1 BOTTLE (72578-007-05)Marketed from Feb 23, 2019
72578-007-2172578000721250 TABLET in 1 BOTTLE (72578-007-21)Marketed from Feb 23, 2019

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)
metronidazole
Generic name (nonproprietary)
metronidazole
Active ingredients
Metronidazole — 250 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 206560
Marketing start
Listing expires
Other FDA classes
Nitroimidazoles (Chemical structure)
Identifiers
Product ID 72578-007_855f53ac-75a4-48d0-9845-1de91708154dSPL ID 855f53ac-75a4-48d0-9845-1de91708154dSPL set ID 0f108035-d2ab-49c1-9f8d-daae11f0efe0RxCUI 311681, 314106UNII 140QMO216E
Pharmacologic class
Nitroimidazole Antimicrobial

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

N472578000701 followed by a unit qualifier and the quantity

Package 72578-0007-01. 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 206560

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

FDA NDC Directory listings under ANDA 206560
ProductStrengthForm · routeLabelerProduct NDC
metronidazoleMetronidazole 250 mg/1TabletOralREMEDYREPACK INC.70518-3042
metronidazoleMetronidazole 500 mg/1TabletOralNorthwind Health Company, LLC82868-014
metronidazoleMetronidazole 500 mg/1TabletOralBryant Ranch Prepack71335-2681
metronidazoleMetronidazole 250 mg/1TabletOralAsclemed USA, Inc.76420-800
metronidazoleMetronidazole 500 mg/1TabletOralAsclemed USA, Inc.76420-801
metronidazoleMetronidazole 500 mg/1TabletOralSportpharm LLC85766-024
metronidazoleMetronidazole 500 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-2409
metronidazoleMetronidazole 500 mg/1TabletOralREMEDYREPACK INC.70518-2663
metronidazoleMetronidazole 500 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-7815
metronidazoleMetronidazole 250 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-195
metronidazoleMetronidazole 500 mg/1TabletOralBryant Ranch Prepack71335-1703
metronidazoleMetronidazole 500 mg/1TabletOralST. MARY'S MEDICAL PARK PHARMACY60760-539
MetronidazoleMetronidazole 500 mg/1TabletOralZydus Lifesciences Limited70771-1046
metronidazoleMetronidazole 500 mg/1TabletOralViona Pharmaceuticals Inc72578-008
MetronidazoleMetronidazole 250 mg/1TabletOralZydus Lifesciences Limited70771-1045
metronidazoleMetronidazole 250 mg/1TabletOralBryant Ranch Prepack71335-1775

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