demeclocycline hydrochloride

Generic: demeclocycline hydrochloride

Labeler: puracap laboratories llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

demeclocycline hydrochloride 300 mg/1

Manufacturer
PuraCap Laboratories LLC

Identifiers & Regulatory

Product NDC 24658-711
Product ID 24658-711_aa40e353-18db-4553-8f8d-a434eac8ed1f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065447
Listing Expiration 2026-12-31
Marketing Start 2017-10-07

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 24658711
Hyphenated Format 24658-711

Supplemental Identifiers

RxCUI
905341 905347
UPC
0324658711485 0324658710013
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
  • 300 mg/1
source: ndc
Packaging
  • 48 TABLET, FILM COATED in 1 BOTTLE (24658-711-48)
source: ndc

Packages (1)

24658-711-48 48 TABLET, FILM COATED in 1 BOTTLE (24658-711-48)

Ingredients (1)

demeclocycline hydrochloride (300 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": "aa40e353-18db-4553-8f8d-a434eac8ed1f", "openfda": {"upc": ["0324658711485", "0324658710013"], "unii": ["29O079NTYT"], "rxcui": ["905341", "905347"], "spl_set_id": ["88e03cb0-25f5-41a5-b77f-58ab8f3be181"], "manufacturer_name": ["PuraCap Laboratories LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "48 TABLET, FILM COATED in 1 BOTTLE (24658-711-48)", "package_ndc": "24658-711-48", "marketing_start_date": "20171007"}], "brand_name": "Demeclocycline Hydrochloride", "product_id": "24658-711_aa40e353-18db-4553-8f8d-a434eac8ed1f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tetracycline-class Antimicrobial [EPC]", "Tetracyclines [CS]"], "product_ndc": "24658-711", "generic_name": "Demeclocycline Hydrochloride", "labeler_name": "PuraCap Laboratories LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Demeclocycline Hydrochloride", "active_ingredients": [{"name": "DEMECLOCYCLINE HYDROCHLORIDE", "strength": "300 mg/1"}], "application_number": "ANDA065447", "marketing_category": "ANDA", "marketing_start_date": "20171007", "listing_expiration_date": "20261231"}