Package 71262-009-01

Brand: tetracyte topical tetracycline hydrochloride

Generic: tetracycline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71262-009-01
Digits Only 7126200901
Product NDC 71262-009
Description

1 BOTTLE in 1 CARTON (71262-009-01) / 15 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2024-05-01
Brand tetracyte topical tetracycline hydrochloride
Generic tetracycline hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "1ea3306d-037f-cb46-e063-6294a90abc20", "openfda": {"upc": ["0860004878209"], "unii": ["P6R62377KV"], "rxcui": ["1542813"], "spl_set_id": ["4ac5177d-bb67-45e6-adcf-44f0821746bd"], "manufacturer_name": ["VIADERMA DISTRIBUTION INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (71262-009-01)  / 15 mL in 1 BOTTLE", "package_ndc": "71262-009-01", "marketing_start_date": "20240501"}], "brand_name": "Tetracyte Topical Tetracycline Hydrochloride", "product_id": "71262-009_1ea3306d-037f-cb46-e063-6294a90abc20", "dosage_form": "OINTMENT", "pharm_class": ["Tetracycline-class Antimicrobial [EPC]", "Tetracyclines [CS]"], "product_ndc": "71262-009", "generic_name": "TETRACYCLINE HYDROCHLORIDE", "labeler_name": "VIADERMA DISTRIBUTION INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Tetracyte Topical Tetracycline Hydrochloride", "active_ingredients": [{"name": "TETRACYCLINE HYDROCHLORIDE", "strength": "30 mg/mL"}], "application_number": "M004", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240501", "listing_expiration_date": "20261231"}