Package 46708-639-31
Brand: doxepin hydrochloride
Generic: doxepin hydrochloridePackage Facts
Identity
Package NDC
46708-639-31
Digits Only
4670863931
Product NDC
46708-639
Description
100 CAPSULE in 1 BOTTLE (46708-639-31)
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": "5c5c56f2-76f7-41b1-8eb5-40dc4cd4ac6a", "openfda": {"upc": ["0346708638313", "0346708639310"], "unii": ["3U9A0FE9N5"], "rxcui": ["1000048", "1000058", "1000070", "1000076", "1000097"], "spl_set_id": ["842b595b-dc54-4898-a178-1d2241cc065f"], "manufacturer_name": ["Alembic Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (46708-639-31)", "package_ndc": "46708-639-31", "marketing_start_date": "20210423"}, {"sample": false, "description": "1000 CAPSULE in 1 BOTTLE (46708-639-91)", "package_ndc": "46708-639-91", "marketing_start_date": "20210423"}], "brand_name": "DOXEPIN HYDROCHLORIDE", "product_id": "46708-639_5c5c56f2-76f7-41b1-8eb5-40dc4cd4ac6a", "dosage_form": "CAPSULE", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "46708-639", "generic_name": "DOXEPIN HYDROCHLORIDE", "labeler_name": "Alembic Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DOXEPIN HYDROCHLORIDE", "active_ingredients": [{"name": "DOXEPIN HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA215076", "marketing_category": "ANDA", "marketing_start_date": "20210423", "listing_expiration_date": "20261231"}