Package 69842-335-28
Brand: guaifenesin
Generic: guaifenesinPackage Facts
Identity
Package NDC
69842-335-28
Digits Only
6984233528
Product NDC
69842-335
Description
28 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (69842-335-28)
Marketing
Marketing Status
Brand
guaifenesin
Generic
guaifenesin
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4653e896-cfea-4625-e063-6394a90a4c7f", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0050428296905"], "unii": ["495W7451VQ"], "rxcui": ["310621"], "spl_set_id": ["bdaf7359-8698-87d6-e053-2a95a90ada28"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["CVS PHARMACY, INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (69842-335-16)", "package_ndc": "69842-335-16", "marketing_start_date": "20210301"}, {"sample": false, "description": "28 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (69842-335-28)", "package_ndc": "69842-335-28", "marketing_start_date": "20210301"}, {"sample": false, "description": "42 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (69842-335-42)", "package_ndc": "69842-335-42", "marketing_start_date": "20210301"}], "brand_name": "Guaifenesin", "product_id": "69842-335_4653e896-cfea-4625-e063-6394a90a4c7f", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "69842-335", "generic_name": "Guaifenesin", "labeler_name": "CVS PHARMACY, INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Guaifenesin", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "1200 mg/1"}], "application_number": "ANDA213420", "marketing_category": "ANDA", "marketing_start_date": "20210301", "listing_expiration_date": "20261231"}