hydrochlorothiazide
Generic: hydrochlorothiazide
Labeler: alembic pharmaceuticals limitedDrug Facts
Product Profile
Brand Name
hydrochlorothiazide
Generic Name
hydrochlorothiazide
Labeler
alembic pharmaceuticals limited
Dosage Form
CAPSULE
Routes
Active Ingredients
hydrochlorothiazide 12.5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
46708-438
Product ID
46708-438_8ed60738-80b1-4c2d-a0f1-cf5fa17f8308
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA200645
Listing Expiration
2026-12-31
Marketing Start
2017-03-02
Pharmacologic Class
Established (EPC)
Chemical Structure
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
46708438
Hyphenated Format
46708-438
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
ANDA200645 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 12.5 mg/1
Packaging
- 10 BLISTER PACK in 1 CARTON (46708-438-10) / 10 CAPSULE in 1 BLISTER PACK
- 30 CAPSULE in 1 BOTTLE (46708-438-30)
- 100 CAPSULE in 1 BOTTLE (46708-438-31)
- 500 CAPSULE in 1 BOTTLE (46708-438-71)
- 1000 CAPSULE in 1 BOTTLE (46708-438-91)
Packages (5)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "8ed60738-80b1-4c2d-a0f1-cf5fa17f8308", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0346708438302"], "unii": ["0J48LPH2TH"], "rxcui": ["199903"], "spl_set_id": ["34703033-14c4-459c-8b8f-2f2e1145aff7"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Alembic Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 CARTON (46708-438-10) / 10 CAPSULE in 1 BLISTER PACK", "package_ndc": "46708-438-10", "marketing_start_date": "20170302"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (46708-438-30)", "package_ndc": "46708-438-30", "marketing_start_date": "20170302"}, {"sample": false, "description": "100 CAPSULE in 1 BOTTLE (46708-438-31)", "package_ndc": "46708-438-31", "marketing_start_date": "20170302"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (46708-438-71)", "package_ndc": "46708-438-71", "marketing_start_date": "20170302"}, {"sample": false, "description": "1000 CAPSULE in 1 BOTTLE (46708-438-91)", "package_ndc": "46708-438-91", "marketing_start_date": "20170302"}], "brand_name": "hydrochlorothiazide", "product_id": "46708-438_8ed60738-80b1-4c2d-a0f1-cf5fa17f8308", "dosage_form": "CAPSULE", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "46708-438", "generic_name": "Hydrochlorothiazide", "labeler_name": "Alembic Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}], "application_number": "ANDA200645", "marketing_category": "ANDA", "marketing_start_date": "20170302", "listing_expiration_date": "20261231"}