NDC codes

FDA NDC Directory
Product NDC (as listed)55154-8190Labeler and product segments. Claims need a package NDC.
Product NDC at billing width55154-8190Add 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
55154-8190-05515481900010 BLISTER PACK in 1 BAG (55154-8190-0) / 1 TABLET in 1 BLISTER PACKMarketed from Feb 20, 2020

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)
Metronidazole
Generic name (nonproprietary)
metronidazole
Active ingredients
Metronidazole — 500 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 070772
Marketing start
Listing expires
Other FDA classes
Nitroimidazoles (Chemical structure)
Identifiers
Product ID 55154-8190_5882576d-a02a-4f0f-ae80-706826268036SPL ID 5882576d-a02a-4f0f-ae80-706826268036
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

N455154819000 followed by a unit qualifier and the quantity

Package 55154-8190-00. 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

The FDA listing for this product does not reference a label (SPL) set.

Other NDCs under ANDA 070772

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

FDA NDC Directory listings under ANDA 070772
ProductStrengthForm · routeLabelerProduct NDC
MetronidazoleMetronidazole 250 mg/1TabletOralAmerican Health Packaging60687-526
metronidazoleMetronidazole 125 mg/1TabletOralBryant Ranch Prepack72162-2468
MetronidazoleMetronidazole 500 mg/1TabletOralAmerican Health Packaging60687-550
metronidazoleMetronidazole 125 mg/1TabletOralMethod Pharmaceuticals LLC58657-739
metronidazoleMetronidazole 125 mg/1TabletOralBryant Ranch Prepack71335-2949
metronidazoleMetronidazole 250 mg/1TabletOralMethod Pharmaceuticals LLC58657-933
metronidazoleMetronidazole 500 mg/1TabletOralMethod Pharmaceuticals LLC58657-934
metronidazoleMetronidazole 125 mg/1TabletOralMethod Pharmaceuticals LLC58657-939
metronidazoleMetronidazole 500 mg/1TabletOralGolden State Medical Supply, Inc.51407-372
metronidazoleMetronidazole 250 mg/1TabletOralGolden State Medical Supply, Inc.51407-376
metronidazoleMetronidazole 250 mg/1TabletOralAMICI PHARMA INC69292-207
metronidazoleMetronidazole 500 mg/1TabletOralAMICI PHARMA INC69292-208

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