tetracycline hydrochloride

Generic: tetracycline hydrochloride

Labeler: preferred pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name tetracycline hydrochloride
Generic Name tetracycline hydrochloride
Labeler preferred pharmaceuticals inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

tetracycline hydrochloride 500 mg/1

Manufacturer
Preferred Pharmaceuticals Inc.

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
tetracycline-class antimicrobial [epc] tetracyclines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687888853
Hyphenated Format 68788-8853

Supplemental Identifiers

RxCUI
198252
UNII
P6R62377KV

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 30 CAPSULE in 1 BOTTLE, PLASTIC (68788-8853-3)
source: ndc

Packages (1)

Ingredients (1)

tetracycline hydrochloride (500 mg/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"}