Package 82644-087-60

Brand: tetracycline hydrochloride

Generic: tetracycline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 82644-087-60
Digits Only 8264408760
Product NDC 82644-087
Product ID 82644-087_3d44a562-4fde-4867-90e6-433ea752bb3c
Description

60 TABLET, FILM COATED in 1 BOTTLE (82644-087-60)

Marketing

Marketing Status
Marketed Since 2024-01-19
Brand tetracycline hydrochloride
Generic tetracycline hydrochloride
Sample Package No

Linked Drug Pages (1)

Tetracycline Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3d44a562-4fde-4867-90e6-433ea752bb3c", "openfda": {"unii": ["P6R62377KV"], "rxcui": ["313252", "313254"], "spl_set_id": ["c522c860-84ce-4c61-ab72-077de73195df"], "manufacturer_name": ["Pharmaka Generics Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (82644-087-60)", "package_ndc": "82644-087-60", "marketing_start_date": "20240119"}], "brand_name": "Tetracycline Hydrochloride", "product_id": "82644-087_3d44a562-4fde-4867-90e6-433ea752bb3c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tetracycline-class Antimicrobial [EPC]", "Tetracyclines [CS]"], "product_ndc": "82644-087", "generic_name": "Tetracycline Hydrochloride", "labeler_name": "Pharmaka Generics Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tetracycline Hydrochloride", "active_ingredients": [{"name": "TETRACYCLINE HYDROCHLORIDE", "strength": "250 mg/1"}], "application_number": "ANDA061147", "marketing_category": "ANDA", "marketing_start_date": "20240119", "listing_expiration_date": "20261231"}