guanfacine hydrochloride

Generic: guanfacine

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name guanfacine hydrochloride
Generic Name guanfacine
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

guanfacine hydrochloride 1 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-6073
Product ID 50090-6073_79615d20-0231-4d1a-a3f5-7037b5d7a4be
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075109
Listing Expiration 2026-12-31
Marketing Start 2022-04-15

Pharmacologic Class

Classes
adrenergic alpha2-agonists [moa] central alpha-2 adrenergic agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500906073
Hyphenated Format 50090-6073

Supplemental Identifiers

RxCUI
197745
UNII
PML56A160O

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 guanfacine hydrochloride (source: ndc)
Generic Name guanfacine (source: ndc)
Application Number ANDA075109 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (50090-6073-0)
source: ndc

Packages (1)

Ingredients (1)

guanfacine hydrochloride (1 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "79615d20-0231-4d1a-a3f5-7037b5d7a4be", "openfda": {"unii": ["PML56A160O"], "rxcui": ["197745"], "spl_set_id": ["9f967d68-5aff-4955-8c79-69febf7c38ad"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-6073-0)", "package_ndc": "50090-6073-0", "marketing_start_date": "20220914"}], "brand_name": "Guanfacine Hydrochloride", "product_id": "50090-6073_79615d20-0231-4d1a-a3f5-7037b5d7a4be", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "50090-6073", "generic_name": "Guanfacine", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Guanfacine Hydrochloride", "active_ingredients": [{"name": "GUANFACINE HYDROCHLORIDE", "strength": "1 mg/1"}], "application_number": "ANDA075109", "marketing_category": "ANDA", "marketing_start_date": "20220415", "listing_expiration_date": "20261231"}