hydrochlorothiazide

Generic: hydrochlorothiazide

Labeler: unichem pharmaceuticals (usa), inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name hydrochlorothiazide
Generic Name hydrochlorothiazide
Labeler unichem pharmaceuticals (usa), inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

hydrochlorothiazide 12.5 mg/1

Manufacturer
Unichem Pharmaceuticals (USA), Inc.

Identifiers & Regulatory

Product NDC 29300-130
Product ID 29300-130_f1b356b8-32c9-43c5-b931-fa67e9b36fb7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090510
Listing Expiration 2026-12-31
Marketing Start 2010-03-15

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 29300130
Hyphenated Format 29300-130

Supplemental Identifiers

RxCUI
199903
UPC
0329300130010
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 ANDA090510 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 12.5 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE, PLASTIC (29300-130-01)
  • 500 CAPSULE in 1 BOTTLE, PLASTIC (29300-130-05)
  • 1000 CAPSULE in 1 BOTTLE, PLASTIC (29300-130-10)
source: ndc

Packages (3)

Ingredients (1)

hydrochlorothiazide (12.5 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f1b356b8-32c9-43c5-b931-fa67e9b36fb7", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0329300130010"], "unii": ["0J48LPH2TH"], "rxcui": ["199903"], "spl_set_id": ["cb7712f3-9a0b-442d-859d-8be5e6e2529a"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Unichem Pharmaceuticals (USA), Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE, PLASTIC (29300-130-01)", "package_ndc": "29300-130-01", "marketing_start_date": "20100315"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE, PLASTIC (29300-130-05)", "package_ndc": "29300-130-05", "marketing_start_date": "20100315"}, {"sample": false, "description": "1000 CAPSULE in 1 BOTTLE, PLASTIC (29300-130-10)", "package_ndc": "29300-130-10", "marketing_start_date": "20100315"}], "brand_name": "hydrochlorothiazide", "product_id": "29300-130_f1b356b8-32c9-43c5-b931-fa67e9b36fb7", "dosage_form": "CAPSULE", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "29300-130", "generic_name": "hydrochlorothiazide", "labeler_name": "Unichem Pharmaceuticals (USA), Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}], "application_number": "ANDA090510", "marketing_category": "ANDA", "marketing_start_date": "20100315", "listing_expiration_date": "20261231"}