guanfacine

Generic: guanfacine

Labeler: major pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name guanfacine
Generic Name guanfacine
Labeler major pharmaceuticals
Dosage Form TABLET
Routes
ORAL
Active Ingredients

guanfacine hydrochloride 1 mg/1

Manufacturer
Major Pharmaceuticals

Identifiers & Regulatory

Product NDC 0904-7140
Product ID 0904-7140_c0b59783-8114-4c3e-bc55-ce8dc849de5e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074673
Listing Expiration 2026-12-31
Marketing Start 2013-12-02

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 09047140
Hyphenated Format 0904-7140

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 (source: ndc)
Generic Name guanfacine (source: ndc)
Application Number ANDA074673 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 30 BLISTER PACK in 1 CARTON (0904-7140-04) / 1 TABLET in 1 BLISTER PACK
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": "c0b59783-8114-4c3e-bc55-ce8dc849de5e", "openfda": {"unii": ["PML56A160O"], "rxcui": ["197745"], "spl_set_id": ["400be431-ad6c-4783-a513-ca8b47bf43ee"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 CARTON (0904-7140-04)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0904-7140-04", "marketing_start_date": "20131202"}], "brand_name": "Guanfacine", "product_id": "0904-7140_c0b59783-8114-4c3e-bc55-ce8dc849de5e", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "0904-7140", "generic_name": "Guanfacine", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Guanfacine", "active_ingredients": [{"name": "GUANFACINE HYDROCHLORIDE", "strength": "1 mg/1"}], "application_number": "ANDA074673", "marketing_category": "ANDA", "marketing_start_date": "20131202", "listing_expiration_date": "20261231"}