Metronidazole

Product NDC
0338-9554
11-digit product format
003389554
Labeler code
0338
Product ID
0338-9554_9e37a540-8657-43e5-9420-a3ea49cd643e
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
metronidazole
Dosage form
INJECTION, SOLUTION
Route
INTRAVENOUS
Labeler
Baxter Healthcare Corporation
Marketing category
UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE
Marketing start
2017-10-05
Marketing end
0000-00-00
Substance
METRONIDAZOLE
Active strength
500 mg/100mL
Pharmacologic classes
Nitroimidazole Antimicrobial [EPC],Nitroimidazoles [CS]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct0338-9554DDiscontinued by firm2026-07-31
excluded packagepackage0338-95540338-9554-50DDiscontinued by firm2026-07-31

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0338-9554-50ML - Milliliter0338-955473c3363c-3f8c-452e-a6df-8182671c77a112017-11-06