Package 37808-068-50
Brand: all day pain relief
Generic: naproxen sodiumPackage Facts
Identity
Package NDC
37808-068-50
Digits Only
3780806850
Product NDC
37808-068
Description
1 BOTTLE, PLASTIC in 1 BOX (37808-068-50) / 50 TABLET in 1 BOTTLE, PLASTIC
Marketing
Marketing Status
Brand
all day pain relief
Generic
naproxen sodium
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "cc1eb980-a014-48df-83cd-9cfa050b4414", "openfda": {"upc": ["0041220284337"], "unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["6dd54a14-67cd-4295-9bd5-1d6f8cb9316d"], "manufacturer_name": ["H E B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (37808-068-24) / 24 TABLET in 1 BOTTLE, PLASTIC", "package_ndc": "37808-068-24", "marketing_start_date": "20150930"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (37808-068-50) / 50 TABLET in 1 BOTTLE, PLASTIC", "package_ndc": "37808-068-50", "marketing_start_date": "20150930"}], "brand_name": "All Day Pain Relief", "product_id": "37808-068_cc1eb980-a014-48df-83cd-9cfa050b4414", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "37808-068", "generic_name": "Naproxen Sodium", "labeler_name": "H E B", "product_type": "HUMAN OTC DRUG", "brand_name_base": "All Day Pain Relief", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA079096", "marketing_category": "ANDA", "marketing_start_date": "20150930", "listing_expiration_date": "20261231"}