Package 37808-112-22

Brand: nasal decongestant

Generic: pseudoephedrine hcl
NDC Package

Package Facts

Identity

Package NDC 37808-112-22
Digits Only 3780811222
Product NDC 37808-112
Description

2 BLISTER PACK in 1 CARTON (37808-112-22) / 24 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 1981-08-25
Brand nasal decongestant
Generic pseudoephedrine hcl
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a2504b24-259a-4ad6-96f3-4a51553aec23", "openfda": {"upc": ["0041220359899"], "unii": ["6V9V2RYJ8N"], "rxcui": ["1049160"], "spl_set_id": ["22d241c5-a3fd-4619-8147-91d7a4c8cf98"], "manufacturer_name": ["H E B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (37808-112-22)  / 24 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "37808-112-22", "marketing_start_date": "19810825"}], "brand_name": "Nasal Decongestant", "product_id": "37808-112_a2504b24-259a-4ad6-96f3-4a51553aec23", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "37808-112", "generic_name": "Pseudoephedrine HCl", "labeler_name": "H E B", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Nasal Decongestant", "active_ingredients": [{"name": "PSEUDOEPHEDRINE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "19810825", "listing_expiration_date": "20271231"}