Package 27808-037-02

{"route": ["ORAL"], "spl_id": "cf89ef14-b1bb-4341-8911-892ce7d157c1", "openfda": {"upc": ["0327808035011", "0327808037015"], "unii": ["NO70W886KK", "362O9ITL9D"], "rxcui": ["856999", "857002", "857005"], "spl_set_id": ["d4caec6d-4af2-4f1c-9add-c0c948b83b16"], "manufacturer_name": ["Cranbury Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (27808-037-01)", "package_ndc": "27808-037-01", "marketing_start_date": "20141006"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (27808-037-02)", "package_ndc": "27808-037-02", "marketing_start_date": "20141006"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (27808-037-03)", "package_ndc": "27808-037-03", "marketing_start_date": "20141006"}], "brand_name": "Hydrocodone Bitartrate and Acetaminophen", "product_id": "27808-037_cf89ef14-b1bb-4341-8911-892ce7d157c1", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "27808-037", "dea_schedule": "CII", "generic_name": "Hydrocodone Bitartrate and Acetaminophen", "labeler_name": "Cranbury Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrocodone Bitartrate and Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "HYDROCODONE BITARTRATE", "strength": "10 mg/1"}], "application_number": "ANDA202214", "marketing_category": "ANDA", "marketing_start_date": "20141006", "listing_expiration_date": "20261231"}