Pantoprazole Sodium

Product NDC: 51655-495
11-digit product format: 516550495
Labeler code: 51655
Product ID: 51655-495_616a2610-d841-74c3-e053-2a91aa0a49d5
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Pantoprazole Sodium
Dosage form: TABLET, DELAYED RELEASE
Route: ORAL
Labeler: Northwind Pharmaceuticals
Application: ANDA078281
Marketing category: ANDA
Marketing start: 2017-12-19
Marketing end: 0000-00-00
Substance: PANTOPRAZOLE SODIUM
Active strength: 40 mg/1
Pharmacologic classes: Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA]
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
51655-495-52	2026-01-05	C162847	48780-1	9d75b9d0-9c52-f424-e053-dadaa90a57ce	616a2610-d840-74c3-e053-2a91aa0a49d5
51655-495-52	2020-01-31	C162847	48780-1	9d75b9d0-9c52-f424-e053-dadaa90a57ce	616a2610-d840-74c3-e053-2a91aa0a49d5

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51655-495	PANTOPRAZOLE SODIUM TABLET, DELAYED RELEASE [NORTHWIND PHARMACEUTICALS]	1	Legacy NDC	20171228_616a2610-d840-74c3-e053-2a91aa0a49d5.zip