Package 51660-492-21

Brand: pseudoephedrine hydrochloride

Generic: pseudoephedrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51660-492-21
Digits Only 5166049221
Product NDC 51660-492
Product ID 51660-492_060dbf55-8c1c-4c02-98e2-83cd6c0bd3fc
Description

20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (51660-492-21)

Marketing

Marketing Status
Marketed Since 2006-04-28
Brand pseudoephedrine hydrochloride
Generic pseudoephedrine hydrochloride
Sample Package No

Linked Drug Pages (1)

Pseudoephedrine hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "060dbf55-8c1c-4c02-98e2-83cd6c0bd3fc", "openfda": {"unii": ["6V9V2RYJ8N"], "rxcui": ["1049154"], "spl_set_id": ["f398ceab-e3d2-421d-813e-b66369f65472"], "manufacturer_name": ["Ohm Laboratories Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (51660-492-21)", "package_ndc": "51660-492-21", "marketing_start_date": "20060428"}], "brand_name": "Pseudoephedrine hydrochloride", "product_id": "51660-492_060dbf55-8c1c-4c02-98e2-83cd6c0bd3fc", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "51660-492", "generic_name": "pseudoephedrine hydrochloride", "labeler_name": "Ohm Laboratories Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pseudoephedrine hydrochloride", "active_ingredients": [{"name": "PSEUDOEPHEDRINE HYDROCHLORIDE", "strength": "120 mg/1"}], "application_number": "ANDA077442", "marketing_category": "ANDA", "marketing_start_date": "20060428", "listing_expiration_date": "20261231"}