Package 69729-322-27
Brand: acetaminophen, chlorpheniramine maleate, phenylephrine hcl
Generic: acetaminophen, chlorpheniramine maleate, phenylephrine hclPackage Facts
Identity
Package NDC
69729-322-27
Digits Only
6972932227
Product NDC
69729-322
Description
2 TABLET in 1 POUCH (69729-322-27)
Marketing
Marketing Status
Brand
acetaminophen, chlorpheniramine maleate, phenylephrine hcl
Generic
acetaminophen, chlorpheniramine maleate, phenylephrine hcl
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d9f8d76e-5f7a-fb3c-e053-2995a90a3125", "openfda": {"upc": ["0856828008137"], "unii": ["362O9ITL9D", "V1Q0O9OJ9Z", "04JA59TNSJ"], "rxcui": ["2463332"], "spl_set_id": ["b3c229a4-c772-70fb-e053-2a95a90a72db"], "manufacturer_name": ["OPMX LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 TABLET in 1 POUCH (69729-322-27)", "package_ndc": "69729-322-27", "marketing_start_date": "20190826"}, {"sample": false, "description": "12 TABLET in 1 POUCH (69729-322-37)", "package_ndc": "69729-322-37", "marketing_start_date": "20190826"}, {"sample": false, "description": "144 TABLET in 1 POUCH (69729-322-38)", "package_ndc": "69729-322-38", "marketing_start_date": "20190826"}], "brand_name": "Acetaminophen, Chlorpheniramine Maleate, Phenylephrine HCl", "product_id": "69729-322_d9f8d76e-5f7a-fb3c-e053-2995a90a3125", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "69729-322", "generic_name": "Acetaminophen, Chlorpheniramine Maleate, Phenylephrine HCl", "labeler_name": "OPMX LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen, Chlorpheniramine Maleate, Phenylephrine HCl", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}, {"name": "CHLORPHENIRAMINE MALEATE", "strength": "4 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190826", "listing_expiration_date": "20261231"}