Package 43386-544-01
Brand: morphine sulfate
Generic: morphine sulfatePackage Facts
Identity
Package NDC
43386-544-01
Digits Only
4338654401
Product NDC
43386-544
Description
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (43386-544-01)
Marketing
Marketing Status
Brand
morphine sulfate
Generic
morphine sulfate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d4efe614-fe99-4cc7-b3ba-87c4e010efbd", "openfda": {"upc": ["0343386542017", "0343386543014", "0343386540013", "0343386541010"], "unii": ["X3P646A2J0"], "rxcui": ["891874", "891881", "891888", "891893", "892646"], "spl_set_id": ["d360a33f-6323-4b10-9e81-07e2813c2dbd"], "manufacturer_name": ["Lupin Pharmaceuticals,Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (43386-544-01)", "package_ndc": "43386-544-01", "marketing_start_date": "20151216"}], "brand_name": "Morphine Sulfate", "product_id": "43386-544_d4efe614-fe99-4cc7-b3ba-87c4e010efbd", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "43386-544", "dea_schedule": "CII", "generic_name": "Morphine Sulfate", "labeler_name": "Lupin Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Morphine Sulfate", "active_ingredients": [{"name": "MORPHINE SULFATE", "strength": "200 mg/1"}], "application_number": "ANDA203602", "marketing_category": "ANDA", "marketing_start_date": "20151216", "listing_expiration_date": "20261231"}