hydrochlorothiazide

Generic: hydrochlorothiazide

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name hydrochlorothiazide
Generic Name hydrochlorothiazide
Labeler remedyrepack inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

hydrochlorothiazide 12.5 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-2550
Product ID 70518-2550_4a667996-17e1-08c3-e063-6394a90ad866
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203561
Listing Expiration 2027-12-31
Marketing Start 2020-01-20

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 705182550
Hyphenated Format 70518-2550

Supplemental Identifiers

RxCUI
199903
UNII
0J48LPH2TH
NUI
N0000175359 N0000175419 M0471776

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
  • 30 CAPSULE in 1 BLISTER PACK (70518-2550-0)
  • 90 CAPSULE in 1 BOTTLE, PLASTIC (70518-2550-1)
  • 60 CAPSULE in 1 BLISTER PACK (70518-2550-2)
source: ndc

Packages (3)

70518-2550-0 30 CAPSULE in 1 BLISTER PACK (70518-2550-0) 70518-2550-1 90 CAPSULE in 1 BOTTLE, PLASTIC (70518-2550-1) 70518-2550-2 60 CAPSULE in 1 BLISTER PACK (70518-2550-2)

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": "4a667996-17e1-08c3-e063-6394a90ad866", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH"], "rxcui": ["199903"], "spl_set_id": ["0789baef-3424-43ab-a3fb-4908172da565"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (70518-2550-0)", "package_ndc": "70518-2550-0", "marketing_start_date": "20200120"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE, PLASTIC (70518-2550-1)", "package_ndc": "70518-2550-1", "marketing_start_date": "20200814"}, {"sample": false, "description": "60 CAPSULE in 1 BLISTER PACK (70518-2550-2)", "package_ndc": "70518-2550-2", "marketing_start_date": "20211206"}], "brand_name": "Hydrochlorothiazide", "product_id": "70518-2550_4a667996-17e1-08c3-e063-6394a90ad866", "dosage_form": "CAPSULE", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "70518-2550", "generic_name": "Hydrochlorothiazide", "labeler_name": "REMEDYREPACK 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": "20200120", "listing_expiration_date": "20271231"}