CEFDINIR

Product NDC: 51655-214
11-digit product format: 516550214
Labeler code: 51655
Product ID: 51655-214_6975ec56-9942-452c-8a09-d6eea291c97d
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: CEFDINIR
Dosage form: CAPSULE
Route: ORAL
Labeler: Northwind Pharmaceuticals, LLC
Application: ANDA065368
Marketing category: ANDA
Marketing start: 2014-09-17
Marketing end: 0000-00-00
Substance: CEFDINIR
Active strength: 300 mg/1
Pharmacologic classes: Cephalosporin Antibacterial [EPC],Cephalosporins [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
51655-214-20	2026-01-13	C162847	48780-1	9d75b9d0-cb7a-f424-e053-dadaa90a57ce	145e4a41-286e-4033-97c4-92d674d7bb89
51655-214-20	2020-01-31	C162847	48780-1	9d75b9d0-cb7a-f424-e053-dadaa90a57ce	145e4a41-286e-4033-97c4-92d674d7bb89

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version	Uploaded
CEFDINIR	ACTIVE INGREDIENT	CI0FAO63WC	CEFDINIR CAPSULE [NORTHWIND PHARMACEUTICALS, LLC]	1
CEFDINIR	ACTIVE MOIETY	CI0FAO63WC	CEFDINIR CAPSULE [NORTHWIND PHARMACEUTICALS, LLC]	1

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51655-214	CEFDINIR CAPSULE [NORTHWIND PHARMACEUTICALS, LLC]	1	Legacy NDC	20140924_145e4a41-286e-4033-97c4-92d674d7bb89.zip