TAMSULOSIN HYDROCHLORIDE

Product NDC: 51655-677
11-digit product format: 516550677
Labeler code: 51655
Product ID: 51655-677_668dc34f-a492-4bca-bed6-e2d2cb0175e3
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: TAMSULOSIN HYDROCHLORIDE
Dosage form: CAPSULE
Route: ORAL
Labeler: Northwind Pharmaceuticals, LLC
Application: ANDA202433
Marketing category: ANDA
Marketing start: 2015-02-27
Marketing end: 0000-00-00
Substance: TAMSULOSIN HYDROCHLORIDE
Active strength: 0 mg/1
Pharmacologic classes: Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC]
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
51655-677-26	2026-01-06	C162847	48780-1	9d75b9d1-0a08-f424-e053-dadaa90a57ce	815595c6-740b-4262-934e-8aa4df073d91
51655-677-26	2020-01-31	C162847	48780-1	9d75b9d1-0a08-f424-e053-dadaa90a57ce	815595c6-740b-4262-934e-8aa4df073d91

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version	Uploaded
TAMSULOSIN HYDROCHLORIDE	ACTIVE INGREDIENT	11SV1951MR	TAMSULOSIN HYDROCHLORIDE CAPSULE [NORTHWIND PHARMACEUTICALS, LLC]	1
TAMSULOSIN	ACTIVE MOIETY	G3P28OML5I	TAMSULOSIN HYDROCHLORIDE CAPSULE [NORTHWIND PHARMACEUTICALS, LLC]	1

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51655-677	TAMSULOSIN HYDROCHLORIDE CAPSULE [NORTHWIND PHARMACEUTICALS, LLC]	1	Legacy NDC	20150320_815595c6-740b-4262-934e-8aa4df073d91.zip