Package 62332-484-71

Brand: doxycycline hyclate

Generic: doxycycline hyclate
NDC Package

Package Facts

Identity

Package NDC 62332-484-71
Digits Only 6233248471
Product NDC 62332-484
Product ID 62332-484_8d58b6bc-d11b-4fa5-91c1-2ddd17bc0388
Description

500 TABLET, DELAYED RELEASE in 1 BOTTLE (62332-484-71)

Marketing

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

Linked Drug Pages (1)

Doxycycline Hyclate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "8d58b6bc-d11b-4fa5-91c1-2ddd17bc0388", "openfda": {"upc": ["0362332483600", "0362332481606", "0362332482603"], "unii": ["19XTS3T51U"], "rxcui": ["406524", "434018", "799048", "1423080"], "spl_set_id": ["3ae4ca12-be39-46b9-bc4c-f8356776c175"], "manufacturer_name": ["Alembic Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (62332-484-30)", "package_ndc": "62332-484-30", "marketing_start_date": "20221015"}, {"sample": false, "description": "100 TABLET, DELAYED RELEASE in 1 BOTTLE (62332-484-31)", "package_ndc": "62332-484-31", "marketing_start_date": "20220104"}, {"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE (62332-484-60)", "package_ndc": "62332-484-60", "marketing_start_date": "20220104"}, {"sample": false, "description": "500 TABLET, DELAYED RELEASE in 1 BOTTLE (62332-484-71)", "package_ndc": "62332-484-71", "marketing_start_date": "20220104"}], "brand_name": "Doxycycline Hyclate", "product_id": "62332-484_8d58b6bc-d11b-4fa5-91c1-2ddd17bc0388", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "62332-484", "generic_name": "Doxycycline Hyclate", "labeler_name": "Alembic Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxycycline Hyclate", "active_ingredients": [{"name": "DOXYCYCLINE HYCLATE", "strength": "200 mg/1"}], "application_number": "ANDA213075", "marketing_category": "ANDA", "marketing_start_date": "20220104", "listing_expiration_date": "20261231"}