demeclocycline hydrochloride

Generic: demeclocycline hydrochloride

Labeler: epic pharma, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name demeclocycline hydrochloride
Generic Name demeclocycline hydrochloride
Labeler epic pharma, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

demeclocycline hydrochloride 150 mg/1

Manufacturer
Epic Pharma, LLC

Identifiers & Regulatory

Product NDC 42806-143
Product ID 42806-143_b84008e7-52db-4b3e-a12e-cb939852ff0f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065447
Listing Expiration 2026-12-31
Marketing Start 2015-02-02

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 42806143
Hyphenated Format 42806-143

Supplemental Identifiers

RxCUI
905341 905347
UPC
0342806144480 0342806143018
UNII
29O079NTYT

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 demeclocycline hydrochloride (source: ndc)
Generic Name demeclocycline hydrochloride (source: ndc)
Application Number ANDA065447 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 150 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (42806-143-01)
  • 500 TABLET, FILM COATED in 1 BOTTLE (42806-143-05)
  • 30 TABLET, FILM COATED in 1 BOTTLE (42806-143-30)
source: ndc

Packages (3)

42806-143-01 100 TABLET, FILM COATED in 1 BOTTLE (42806-143-01) 42806-143-05 500 TABLET, FILM COATED in 1 BOTTLE (42806-143-05) 42806-143-30 30 TABLET, FILM COATED in 1 BOTTLE (42806-143-30)

Ingredients (1)

demeclocycline hydrochloride (150 mg/1)

Linked Drug Pages (1)

Demeclocycline Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "b84008e7-52db-4b3e-a12e-cb939852ff0f", "openfda": {"upc": ["0342806144480", "0342806143018"], "unii": ["29O079NTYT"], "rxcui": ["905341", "905347"], "spl_set_id": ["645af8f4-0843-4afb-9ddc-f587f38adb68"], "manufacturer_name": ["Epic Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (42806-143-01)", "package_ndc": "42806-143-01", "marketing_start_date": "20150202"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (42806-143-05)", "package_ndc": "42806-143-05", "marketing_start_date": "20150202"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (42806-143-30)", "package_ndc": "42806-143-30", "marketing_start_date": "20150202"}], "brand_name": "Demeclocycline Hydrochloride", "product_id": "42806-143_b84008e7-52db-4b3e-a12e-cb939852ff0f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tetracycline-class Antimicrobial [EPC]", "Tetracyclines [CS]"], "product_ndc": "42806-143", "generic_name": "Demeclocycline Hydrochloride", "labeler_name": "Epic Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Demeclocycline Hydrochloride", "active_ingredients": [{"name": "DEMECLOCYCLINE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA065447", "marketing_category": "ANDA", "marketing_start_date": "20150202", "listing_expiration_date": "20261231"}