Package 0113-0401-62

Brand: zephrex d

Generic: pseudoephedrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0113-0401-62
Digits Only 0113040162
Product NDC 0113-0401
Product ID 0113-0401_28086f51-f7d5-4c69-ad06-49aa164db301
Description

24 BLISTER PACK in 1 CARTON (0113-0401-62) / 1 CAPSULE, GELATIN COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2017-04-17
Brand zephrex d
Generic pseudoephedrine hydrochloride
Sample Package No

Linked Drug Pages (1)

Zephrex D ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "28086f51-f7d5-4c69-ad06-49aa164db301", "openfda": {"unii": ["6V9V2RYJ8N"], "rxcui": ["1430169", "1918218"], "spl_set_id": ["5468a7e2-361b-494f-9ca3-1b62f3819f65"], "manufacturer_name": ["L. Perrigo Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 BLISTER PACK in 1 CARTON (0113-0401-62)  / 1 CAPSULE, GELATIN COATED in 1 BLISTER PACK", "package_ndc": "0113-0401-62", "marketing_start_date": "20170417"}, {"sample": false, "description": "48 BLISTER PACK in 1 CARTON (0113-0401-67)  / 1 CAPSULE, GELATIN COATED in 1 BLISTER PACK", "package_ndc": "0113-0401-67", "marketing_start_date": "20170508"}], "brand_name": "Zephrex D", "product_id": "0113-0401_28086f51-f7d5-4c69-ad06-49aa164db301", "dosage_form": "CAPSULE, GELATIN COATED", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "0113-0401", "generic_name": "pseudoephedrine hydrochloride", "labeler_name": "L. Perrigo Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Zephrex D", "active_ingredients": [{"name": "PSEUDOEPHEDRINE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20161104", "listing_expiration_date": "20261231"}