Package 23155-893-31
Brand: methohexital sodium
Generic: methohexital sodiumPackage Facts
Identity
Package NDC
23155-893-31
Digits Only
2315589331
Product NDC
23155-893
Description
1 VIAL in 1 CARTON (23155-893-31) / 500 mg in 1 VIAL
Marketing
Marketing Status
Brand
methohexital sodium
Generic
methohexital sodium
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS", "RECTAL"], "spl_id": "9ec15df7-278e-4cf3-bc97-e480b4671ca6", "openfda": {"upc": ["0323155893311", "0011100004492"], "unii": ["60200PNZ7Q"], "rxcui": ["1244233"], "spl_set_id": ["f76d4ab9-2f6c-420b-afec-b9cdfdc083ce"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (23155-893-31) / 500 mg in 1 VIAL", "package_ndc": "23155-893-31", "marketing_start_date": "20241212"}], "brand_name": "Methohexital Sodium", "product_id": "23155-893_9ec15df7-278e-4cf3-bc97-e480b4671ca6", "dosage_form": "INJECTION", "pharm_class": ["Barbiturate [EPC]", "Barbiturates [CS]"], "product_ndc": "23155-893", "dea_schedule": "CIV", "generic_name": "Methohexital Sodium", "labeler_name": "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methohexital Sodium", "active_ingredients": [{"name": "METHOHEXITAL SODIUM", "strength": "500 mg/500mg"}], "application_number": "ANDA215488", "marketing_category": "ANDA", "marketing_start_date": "20241212", "listing_expiration_date": "20261231"}