tetracycline hydrochloride
Generic: tetracycline hydrochloride
Labeler: preferred pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
tetracycline hydrochloride
Generic Name
tetracycline hydrochloride
Labeler
preferred pharmaceuticals inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
tetracycline hydrochloride 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68788-8853
Product ID
68788-8853_4202cbfb-52e9-47f2-bd3a-1003319ca3cb
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA061837
Listing Expiration
2026-12-31
Marketing Start
2025-03-24
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
687888853
Hyphenated Format
68788-8853
Supplemental Identifiers
RxCUI
UNII
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
tetracycline hydrochloride (source: ndc)
Generic Name
tetracycline hydrochloride (source: ndc)
Application Number
ANDA061837 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 30 CAPSULE in 1 BOTTLE, PLASTIC (68788-8853-3)
Packages (1)
Ingredients (1)
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"}