Package 62332-637-31
Brand: doxepin hydrochloride
Generic: doxepin hydrochloridePackage Facts
Identity
Package NDC
62332-637-31
Digits Only
6233263731
Product NDC
62332-637
Description
100 CAPSULE in 1 BOTTLE (62332-637-31)
Marketing
Marketing Status
Brand
doxepin hydrochloride
Generic
doxepin hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c3977b05-a9fc-4cc4-adfc-731abe6613dd", "openfda": {"upc": ["0362332645312"], "unii": ["3U9A0FE9N5"], "rxcui": ["1000048", "1000058", "1000070", "1000076", "1000097"], "spl_set_id": ["4920401a-cde5-404b-82aa-c3c0e8911065"], "manufacturer_name": ["Alembic Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (62332-637-31)", "package_ndc": "62332-637-31", "marketing_start_date": "20210423"}, {"sample": false, "description": "1000 CAPSULE in 1 BOTTLE (62332-637-91)", "package_ndc": "62332-637-91", "marketing_start_date": "20210423"}], "brand_name": "DOXEPIN HYDROCHLORIDE", "product_id": "62332-637_c3977b05-a9fc-4cc4-adfc-731abe6613dd", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "62332-637", "generic_name": "DOXEPIN HYDROCHLORIDE", "labeler_name": "Alembic Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DOXEPIN HYDROCHLORIDE", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA215076", "marketing_category": "ANDA", "marketing_start_date": "20210423", "listing_expiration_date": "20261231"}