Package 37808-007-69

Brand: pseudoephedrine hydrochloride

Generic: pseudoephedrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 37808-007-69
Digits Only 3780800769
Product NDC 37808-007
Product ID 37808-007_66766915-1aef-4c72-8f47-f6074d2ab1ac
Description

1 BLISTER PACK in 1 CARTON (37808-007-69) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2019-05-15
Brand pseudoephedrine hydrochloride
Generic pseudoephedrine hydrochloride
Sample Package No

Linked Drug Pages (1)

Pseudoephedrine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "66766915-1aef-4c72-8f47-f6074d2ab1ac", "openfda": {"unii": ["6V9V2RYJ8N"], "rxcui": ["1049154"], "spl_set_id": ["d9b46ff2-8bde-47c0-bc63-b19dbe7e197b"], "manufacturer_name": ["HEB"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (37808-007-69)  / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "37808-007-69", "marketing_start_date": "20190515"}], "brand_name": "Pseudoephedrine Hydrochloride", "product_id": "37808-007_66766915-1aef-4c72-8f47-f6074d2ab1ac", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "37808-007", "generic_name": "Pseudoephedrine Hydrochloride", "labeler_name": "HEB", "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": "20190515", "listing_expiration_date": "20261231"}