hydrochlorothiazide
Generic: hydrochlorothiazide
Labeler: unichem pharmaceuticals (usa), inc.Drug Facts
Product Profile
Brand Name
hydrochlorothiazide
Generic Name
hydrochlorothiazide
Labeler
unichem pharmaceuticals (usa), inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
hydrochlorothiazide 12.5 mg/1
Manufacturer
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)
Chemical Structure
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
29300130
Hyphenated Format
29300-130
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 12.5 mg/1
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)
Packages (3)
Ingredients (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"}