Package 70748-338-10

Brand: doxycycline

Generic: doxycycline
NDC Package

Package Facts

Identity

Package NDC 70748-338-10
Digits Only 7074833810
Product NDC 70748-338
Product ID 70748-338_63341990-2dfb-45e9-b1a5-00e529e83661
Description

10 VIAL in 1 CARTON (70748-338-10) / 10 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2024-05-31
Brand doxycycline
Generic doxycycline
Sample Package No

Linked Drug Pages (1)

DOXYCYCLINE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "63341990-2dfb-45e9-b1a5-00e529e83661", "openfda": {"unii": ["19XTS3T51U"], "rxcui": ["310027"], "spl_set_id": ["2946fc05-78e5-4669-85d1-3a3979eceae0"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (70748-338-10)  / 10 mL in 1 VIAL", "package_ndc": "70748-338-10", "marketing_start_date": "20240531"}], "brand_name": "DOXYCYCLINE", "product_id": "70748-338_63341990-2dfb-45e9-b1a5-00e529e83661", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "70748-338", "generic_name": "doxycycline", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DOXYCYCLINE", "active_ingredients": [{"name": "DOXYCYCLINE HYCLATE", "strength": "100 mg/10mL"}], "application_number": "ANDA217794", "marketing_category": "ANDA", "marketing_start_date": "20240531", "listing_expiration_date": "20261231"}