Package 70677-1019-1
Brand: pseudoephedrine hydrochloride
Generic: pseudoephedrine hydrochloridePackage Facts
Identity
Package NDC
70677-1019-1
Digits Only
7067710191
Product NDC
70677-1019
Description
1 BLISTER PACK in 1 CARTON (70677-1019-1) / 10 TABLET, FILM COATED in 1 BLISTER PACK
Marketing
Marketing Status
Brand
pseudoephedrine hydrochloride
Generic
pseudoephedrine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a8f13ce3-e26c-4c8e-9946-bcc08d1a64bb", "openfda": {"unii": ["6V9V2RYJ8N"], "rxcui": ["1049154"], "spl_set_id": ["3bf95c58-4fd9-4caa-a54f-2e61a5eacae8"], "manufacturer_name": ["STRATEGIC SOURCING SERVICES LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (70677-1019-1) / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "70677-1019-1", "marketing_start_date": "20230810"}], "brand_name": "Pseudoephedrine hydrochloride", "product_id": "70677-1019_a8f13ce3-e26c-4c8e-9946-bcc08d1a64bb", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "70677-1019", "generic_name": "Pseudoephedrine hydrochloride", "labeler_name": "STRATEGIC SOURCING SERVICES LLC", "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": "20230810", "listing_expiration_date": "20261231"}