Package 60687-705-65

Brand: demeclocycline hydrochloride

Generic: demeclocycline
NDC Package

Package Facts

Identity

Package NDC 60687-705-65
Digits Only 6068770565
Product NDC 60687-705
Product ID 60687-705_230a18ee-ef80-61c6-e063-6394a90acb5d
Description

50 BLISTER PACK in 1 CARTON (60687-705-65) / 1 TABLET in 1 BLISTER PACK (60687-705-11)

Marketing

Marketing Status
Marketed Since 2023-01-19
Brand demeclocycline hydrochloride
Generic demeclocycline
Sample Package No

Linked Drug Pages (1)

Demeclocycline Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "230a18ee-ef80-61c6-e063-6394a90acb5d", "openfda": {"unii": ["29O079NTYT"], "rxcui": ["905341", "905347"], "spl_set_id": ["e6adaf70-5ff9-4395-bff1-0f332090cb80"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 CARTON (60687-705-65)  / 1 TABLET in 1 BLISTER PACK (60687-705-11)", "package_ndc": "60687-705-65", "marketing_start_date": "20230119"}], "brand_name": "Demeclocycline Hydrochloride", "product_id": "60687-705_230a18ee-ef80-61c6-e063-6394a90acb5d", "dosage_form": "TABLET", "pharm_class": ["Tetracycline-class Antimicrobial [EPC]", "Tetracyclines [CS]"], "product_ndc": "60687-705", "generic_name": "Demeclocycline", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Demeclocycline Hydrochloride", "active_ingredients": [{"name": "DEMECLOCYCLINE HYDROCHLORIDE", "strength": "300 mg/1"}], "application_number": "ANDA065425", "marketing_category": "ANDA", "marketing_start_date": "20230119", "listing_expiration_date": "20261231"}