Package 46708-481-91

Brand: doxycycline hyclate

Generic: doxycycline hyclate
NDC Package

Package Facts

Identity

Package NDC 46708-481-91
Digits Only 4670848191
Product NDC 46708-481
Description

1000 TABLET, DELAYED RELEASE in 1 BOTTLE (46708-481-91)

Marketing

Marketing Status
Marketed Since 2022-01-04
Brand doxycycline hyclate
Generic doxycycline hyclate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e1387662-e286-469d-b85f-60344918a17b", "openfda": {"upc": ["0346708483609", "0346708482602", "0346708481605", "0346708484606"], "unii": ["19XTS3T51U"], "rxcui": ["406524", "434018", "799048", "1423080"], "spl_set_id": ["44ac5de1-c0c6-4d58-9a49-b2dae60ea921"], "manufacturer_name": ["Alembic Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, DELAYED RELEASE in 1 BOTTLE (46708-481-31)", "package_ndc": "46708-481-31", "marketing_start_date": "20220104"}, {"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE (46708-481-60)", "package_ndc": "46708-481-60", "marketing_start_date": "20220104"}, {"sample": false, "description": "1000 TABLET, DELAYED RELEASE in 1 BOTTLE (46708-481-91)", "package_ndc": "46708-481-91", "marketing_start_date": "20220104"}], "brand_name": "Doxycycline Hyclate", "product_id": "46708-481_e1387662-e286-469d-b85f-60344918a17b", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "46708-481", "generic_name": "Doxycycline Hyclate", "labeler_name": "Alembic Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxycycline Hyclate", "active_ingredients": [{"name": "DOXYCYCLINE HYCLATE", "strength": "75 mg/1"}], "application_number": "ANDA213075", "marketing_category": "ANDA", "marketing_start_date": "20220104", "listing_expiration_date": "20261231"}