Package 68788-8853-3

Brand: tetracycline hydrochloride

Generic: tetracycline hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68788-8853-3
Digits Only 6878888533
Product NDC 68788-8853
Description

30 CAPSULE in 1 BOTTLE, PLASTIC (68788-8853-3)

Marketing

Marketing Status
Marketed Since 2025-03-24
Brand tetracycline hydrochloride
Generic tetracycline hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4202cbfb-52e9-47f2-bd3a-1003319ca3cb", "openfda": {"unii": ["P6R62377KV"], "rxcui": ["198252"], "spl_set_id": ["4202cbfb-52e9-47f2-bd3a-1003319ca3cb"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE, PLASTIC (68788-8853-3)", "package_ndc": "68788-8853-3", "marketing_start_date": "20250324"}], "brand_name": "Tetracycline Hydrochloride", "product_id": "68788-8853_4202cbfb-52e9-47f2-bd3a-1003319ca3cb", "dosage_form": "CAPSULE", "pharm_class": ["Tetracycline-class Antimicrobial [EPC]", "Tetracyclines [CS]"], "product_ndc": "68788-8853", "generic_name": "Tetracycline Hydrochloride", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tetracycline Hydrochloride", "active_ingredients": [{"name": "TETRACYCLINE HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA061837", "marketing_category": "ANDA", "marketing_start_date": "20250324", "listing_expiration_date": "20261231"}