Package 46708-316-31
Brand: desipramine hydrochloride
Generic: desipramine hydrochloridePackage Facts
Identity
Package NDC
46708-316-31
Digits Only
4670831631
Product NDC
46708-316
Description
100 TABLET, FILM COATED in 1 BOTTLE (46708-316-31)
Marketing
Marketing Status
Brand
desipramine hydrochloride
Generic
desipramine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "878a2586-20af-4f35-8908-82474cc732a3", "openfda": {"upc": ["0346708315306"], "unii": ["1Y58DO4MY1"], "rxcui": ["1099288", "1099292", "1099296", "1099300", "1099304", "1099316"], "spl_set_id": ["8b6d2289-aac9-4007-a73d-c168fd2e1d9e"], "manufacturer_name": ["Alembic Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (46708-316-30)", "package_ndc": "46708-316-30", "marketing_start_date": "20210708"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (46708-316-31)", "package_ndc": "46708-316-31", "marketing_start_date": "20210708"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (46708-316-91)", "package_ndc": "46708-316-91", "marketing_start_date": "20210708"}], "brand_name": "DESIPRAMINE HYDROCHLORIDE", "product_id": "46708-316_878a2586-20af-4f35-8908-82474cc732a3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "46708-316", "generic_name": "DESIPRAMINE HYDROCHLORIDE", "labeler_name": "Alembic Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DESIPRAMINE HYDROCHLORIDE", "active_ingredients": [{"name": "DESIPRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA209785", "marketing_category": "ANDA", "marketing_start_date": "20210708", "listing_expiration_date": "20261231"}