METRONIDAZOLE

Product NDC: 51655-189
11-digit product format: 516550189
Labeler code: 51655
Product ID: 51655-189_49502689-685c-4fd3-b1a4-3d1f76d61581
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: METRONIDAZOLE
Dosage form: TABLET
Route: ORAL
Labeler: Northwind Pharmaceuticals, LLC
Application: ANDA070033
Marketing category: ANDA
Marketing start: 2014-09-17
Marketing end: 0000-00-00
Substance: METRONIDAZOLE
Active strength: 500 mg/1
Pharmacologic classes: Nitroimidazole Antimicrobial [EPC],Nitroimidazoles [CS]
NDC exclude flag: No
Listing certified through: 2019-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
51655-189-84	2026-01-06	C162847	48780-1	9d75b9d1-2349-f424-e053-dadaa90a57ce	2d5adacb-cd13-4be5-9e2c-c129d45f1c67
51655-189-84	2020-01-31	C162847	48780-1	9d75b9d1-2349-f424-e053-dadaa90a57ce	2d5adacb-cd13-4be5-9e2c-c129d45f1c67

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51655-189	METRONIDAZOLE TABLET [NORTHWIND PHARMACEUTICALS, LLC]	1	Legacy NDC	20140924_2d5adacb-cd13-4be5-9e2c-c129d45f1c67.zip