Package 70069-381-10
Brand: haloperidol decanoate
Generic: haloperidol decanoatePackage Facts
Identity
Package NDC
70069-381-10
Digits Only
7006938110
Product NDC
70069-381
Description
10 VIAL, SINGLE-DOSE in 1 CARTON (70069-381-10) / 1 mL in 1 VIAL, SINGLE-DOSE
Marketing
Marketing Status
Brand
haloperidol decanoate
Generic
haloperidol decanoate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR"], "spl_id": "f6d888a0-65a7-4073-8671-b00b4bfaff4c", "openfda": {"upc": ["0370069382011", "0370069383018", "0370069031018", "0370069030011", "0370069384015"], "unii": ["AC20PJ4101"], "rxcui": ["859867", "859871", "1719803", "1719862"], "spl_set_id": ["f2bff27f-929f-4f7d-b3eb-084ebc2a885f"], "manufacturer_name": ["Somerset Therapeutics, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (70069-381-01) / 1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "70069-381-01", "marketing_start_date": "20191004"}, {"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (70069-381-10) / 1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "70069-381-10", "marketing_start_date": "20190404"}], "brand_name": "HALOPERIDOL DECANOATE", "product_id": "70069-381_f6d888a0-65a7-4073-8671-b00b4bfaff4c", "dosage_form": "INJECTION", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "70069-381", "generic_name": "HALOPERIDOL DECANOATE", "labeler_name": "Somerset Therapeutics, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HALOPERIDOL DECANOATE", "active_ingredients": [{"name": "HALOPERIDOL DECANOATE", "strength": "50 mg/mL"}], "application_number": "ANDA209101", "marketing_category": "ANDA", "marketing_start_date": "20190404", "listing_expiration_date": "20261231"}