Probenecid

Product NDC: 69367-154
11-digit product format: 693670154
Labeler code: 69367
Product ID: 69367-154_38a2d4c1-e32a-2dbb-e054-00144ff8d46c
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Probenecid
Dosage form: TABLET
Route: ORAL
Labeler: Westminster Pharmaceuticals, LLC
Application: ANDA084442
Marketing category: ANDA
Marketing start: 2016-07-28
Marketing end: 0000-00-00
Substance: PROBENECID
Active strength: 500 mg/1
NDC exclude flag: E
Listing certified through: 2018-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
69367-154-00	2020-01-31	C162847	48780-1	9d75b9d0-c59b-f424-e053-dadaa90a57ce	38a2d4c1-e329-2dbb-e054-00144ff8d46c

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
69367-154	PROBENECID TABLET [WESTMINSTER PHARMACEUTICALS, LLC]	1	Legacy NDC	20160729_38a2d4c1-e329-2dbb-e054-00144ff8d46c.zip