Package 64380-225-01

Brand: DOXYCYCLINE HYCLATE

Generic: DOXYCYCLINE HYCLATE
NDC Package

Package Facts

Identity

Package NDC 64380-225-01
Digits Only 6438022501
Product NDC 64380-225
Description

60 TABLET in 1 BOTTLE (64380-225-01)

Marketing

Marketing Status
Marketed Since 2026-01-01
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": "ee86fb38-78c9-4e94-9c94-36ff79051063", "openfda": {"upc": ["0364380225010"], "unii": ["19XTS3T51U"], "rxcui": ["1652674"], "spl_set_id": ["2deeee4f-b342-a178-e063-6394a90af897"], "manufacturer_name": ["Strides Pharma Science Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (64380-225-01)", "package_ndc": "64380-225-01", "marketing_start_date": "20260101"}], "brand_name": "DOXYCYCLINE HYCLATE", "product_id": "64380-225_ee86fb38-78c9-4e94-9c94-36ff79051063", "dosage_form": "TABLET", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "64380-225", "generic_name": "DOXYCYCLINE HYCLATE", "labeler_name": "Strides Pharma Science Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DOXYCYCLINE HYCLATE", "active_ingredients": [{"name": "DOXYCYCLINE HYCLATE", "strength": "50 mg/1"}], "application_number": "ANDA062538", "marketing_category": "ANDA", "marketing_start_date": "20260101", "listing_expiration_date": "20261231"}