hydrochlorothiazide

Generic: hydrochlorothiazide

Labeler: sciegen pharmaceuticals inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name hydrochlorothiazide
Generic Name hydrochlorothiazide
Labeler sciegen pharmaceuticals inc
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

hydrochlorothiazide 12.5 mg/1

Manufacturer
ScieGen Pharmaceuticals Inc

Identifiers & Regulatory

Product NDC 50228-146
Product ID 50228-146_6847f060-0180-4f7e-aba8-4dce8c53e7ae
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203561
Listing Expiration 2027-12-31
Marketing Start 2019-01-14

Pharmacologic Class

Established (EPC)
thiazide diuretic [epc]
Chemical Structure
thiazides [cs]
Physiologic Effect
increased diuresis [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 50228146
Hyphenated Format 50228-146

Supplemental Identifiers

RxCUI
199903
UPC
0350228146012
UNII
0J48LPH2TH
NUI
N0000175359 N0000175419 M0471776

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 hydrochlorothiazide (source: ndc)
Generic Name hydrochlorothiazide (source: ndc)
Application Number ANDA203561 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 12.5 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (50228-146-01)
  • 500 CAPSULE in 1 BOTTLE (50228-146-05)
  • 1000 CAPSULE in 1 BOTTLE (50228-146-10)
  • 30 CAPSULE in 1 BOTTLE (50228-146-30)
source: ndc

Packages (4)

50228-146-01 100 CAPSULE in 1 BOTTLE (50228-146-01) 50228-146-05 500 CAPSULE in 1 BOTTLE (50228-146-05) 50228-146-10 1000 CAPSULE in 1 BOTTLE (50228-146-10) 50228-146-30 30 CAPSULE in 1 BOTTLE (50228-146-30)

Ingredients (1)

hydrochlorothiazide (12.5 mg/1)

Linked Drug Pages (1)

Hydrochlorothiazide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "6847f060-0180-4f7e-aba8-4dce8c53e7ae", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0350228146012"], "unii": ["0J48LPH2TH"], "rxcui": ["199903"], "spl_set_id": ["911a18c1-120a-46b3-b7a8-25eb37843473"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["ScieGen Pharmaceuticals Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (50228-146-01)", "package_ndc": "50228-146-01", "marketing_start_date": "20190114"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (50228-146-05)", "package_ndc": "50228-146-05", "marketing_start_date": "20190114"}, {"sample": false, "description": "1000 CAPSULE in 1 BOTTLE (50228-146-10)", "package_ndc": "50228-146-10", "marketing_start_date": "20190114"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (50228-146-30)", "package_ndc": "50228-146-30", "marketing_start_date": "20190114"}], "brand_name": "Hydrochlorothiazide", "product_id": "50228-146_6847f060-0180-4f7e-aba8-4dce8c53e7ae", "dosage_form": "CAPSULE", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "50228-146", "generic_name": "Hydrochlorothiazide", "labeler_name": "ScieGen Pharmaceuticals Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}], "application_number": "ANDA203561", "marketing_category": "ANDA", "marketing_start_date": "20190114", "listing_expiration_date": "20271231"}