tetracycline hydrochloride

Generic: tetracycline hydrochloride

Labeler: pharmaka generics inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name tetracycline hydrochloride
Generic Name tetracycline hydrochloride
Labeler pharmaka generics inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

tetracycline hydrochloride 250 mg/1

Manufacturer
Pharmaka Generics Inc.

Identifiers & Regulatory

Product NDC 82644-087
Product ID 82644-087_3d44a562-4fde-4867-90e6-433ea752bb3c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA061147
Listing Expiration 2026-12-31
Marketing Start 2024-01-19

Pharmacologic Class

Classes
tetracycline-class antimicrobial [epc] tetracyclines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 82644087
Hyphenated Format 82644-087

Supplemental Identifiers

RxCUI
313252 313254
UNII
P6R62377KV

Packaging Origin

Original Packager
true

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 ANDA061147 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
source: ndc
Packaging
  • 60 TABLET, FILM COATED in 1 BOTTLE (82644-087-60)
source: ndc

Packages (1)

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

Ingredients (1)

tetracycline hydrochloride (250 mg/1)

Linked Drug Pages (1)

Tetracycline Hydrochloride ndc-match (0.9)

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"}