NDC 43547-397

Hydrochlorothiazide

Hydrochlorothiazide

Hydrochlorothiazide is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Solco Healthcare U.s., Llc. The primary component is Hydrochlorothiazide.

Product ID43547-397_ba6274f4-af1c-42cf-b72f-a4371c225da8
NDC43547-397
Product TypeHuman Prescription Drug
Proprietary NameHydrochlorothiazide
Generic NameHydrochlorothiazide
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2002-03-29
Marketing CategoryANDA / ANDA
Application NumberANDA040412
Labeler NameSolco Healthcare U.S., LLC
Substance NameHYDROCHLOROTHIAZIDE
Active Ingredient Strength25 mg/1
Pharm ClassesIncreased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 43547-397-01

10 TABLET in 1 BOTTLE, PLASTIC (43547-397-01)
Marketing Start Date2002-03-29
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 43547-397-11 [43547039711]

Hydrochlorothiazide TABLET
Marketing CategoryANDA
Application NumberANDA040412
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2002-03-29

NDC 43547-397-03 [43547039703]

Hydrochlorothiazide TABLET
Marketing CategoryANDA
Application NumberANDA040412
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2002-03-29

NDC 43547-397-05 [43547039705]

Hydrochlorothiazide TABLET
Marketing CategoryANDA
Application NumberANDA040412
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2002-03-29

NDC 43547-397-10 [43547039710]

Hydrochlorothiazide TABLET
Marketing CategoryANDA
Application NumberANDA040412
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2002-03-29

NDC 43547-397-50 [43547039750]

Hydrochlorothiazide TABLET
Marketing CategoryANDA
Application NumberANDA040412
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2002-03-29

NDC 43547-397-01 [43547039701]

Hydrochlorothiazide TABLET
Marketing CategoryANDA
Application NumberANDA040412
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2002-03-29

NDC 43547-397-15 [43547039715]

Hydrochlorothiazide TABLET
Marketing CategoryANDA
Application NumberANDA040412
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2002-03-29

Drug Details

Active Ingredients

IngredientStrength
HYDROCHLOROTHIAZIDE25 mg/1

OpenFDA Data

SPL SET ID:60c97ab9-b25e-4ea5-a159-792292178c65
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 310798
  • 197770

    • Pharmacological Class

    • Increased Diuresis [PE]
    • Thiazide Diuretic [EPC]
    • Thiazides [CS]
    • Increased Diuresis [PE]
    • Thiazide Diuretic [EPC]
    • Thiazides [CS]

    Medicade Reported Pricing

    43547039711 HYDROCHLOROTHIAZIDE 25 MG TAB

    Pricing Unit: EA | Drug Type:

    43547039710 HYDROCHLOROTHIAZIDE 25 MG TAB

    Pricing Unit: EA | Drug Type:

    NDC Crossover Matching brand name "Hydrochlorothiazide" or generic name "Hydrochlorothiazide"

    NDCBrand NameGeneric Name
    0143-1256HydrochlorothiazideHydrochlorothiazide
    0143-1257HydrochlorothiazideHydrochlorothiazide
    0143-3125HydrochlorothiazideHydrochlorothiazide
    0172-2083HydrochlorothiazideHydrochlorothiazide
    0172-2089HydrochlorothiazideHydrochlorothiazide
    0179-0065HydrochlorothiazideHydrochlorothiazide
    0228-2820HydrochlorothiazideHydrochlorothiazide
    0378-0810Hydrochlorothiazidehydrochlorothiazide
    0440-1595HydrochlorothiazideHydrochlorothiazide
    0440-7595HydrochlorothiazideHydrochlorothiazide
    0527-1413HydrochlorothiazideHydrochlorothiazide
    0527-1414HydrochlorothiazideHydrochlorothiazide
    0527-1635HydrochlorothiazideHydrochlorothiazide
    0591-0347HydrochlorothiazideHydrochlorothiazide
    0615-1358HydrochlorothiazideHydrochlorothiazide
    0615-1561HydrochlorothiazideHydrochlorothiazide
    0615-1562HydrochlorothiazideHydrochlorothiazide
    0615-7974HydrochlorothiazideHydrochlorothiazide
    0615-8036Hydrochlorothiazidehydrochlorothiazide
    0615-8149HydrochlorothiazideHydrochlorothiazide
    0615-8344HydrochlorothiazideHydrochlorothiazide
    10544-028HydrochlorothiazideHydrochlorothiazide
    10544-047HydrochlorothiazideHydrochlorothiazide
    10544-105HydrochlorothiazideHydrochlorothiazide
    10544-136HydrochlorothiazideHydrochlorothiazide
    10544-197HydrochlorothiazideHydrochlorothiazide
    10544-198HydrochlorothiazideHydrochlorothiazide
    68071-1255hydrochlorothiazidehydrochlorothiazide
    68071-1736HYDROCHLOROTHIAZIDEHYDROCHLOROTHIAZIDE
    68071-3238HydrochlorothiazideHydrochlorothiazide
    68071-3215HYDROCHLOROTHIAZIDEHYDROCHLOROTHIAZIDE
    68071-3323HydrochlorothiazideHydrochlorothiazide
    68071-4176HydrochlorothiazideHydrochlorothiazide
    68071-4361HydrochlorothiazideHydrochlorothiazide
    68071-4438HydrochlorothiazideHydrochlorothiazide
    68071-4819HydrochlorothiazideHydrochlorothiazide
    68071-4807HydrochlorothiazideHydrochlorothiazide
    68071-4758HydrochlorothiazideHydrochlorothiazide
    68151-2757HydrochlorothiazideHydrochlorothiazide
    68151-2781HydrochlorothiazideHydrochlorothiazide
    68645-340HydrochlorothiazideHydrochlorothiazide
    68645-341HydrochlorothiazideHydrochlorothiazide
    68645-511HydrochlorothiazideHydrochlorothiazide
    68645-510HydrochlorothiazideHydrochlorothiazide
    68788-6844HydrochlorothiazideHydrochlorothiazide
    68788-8928HydrochlorothiazideHydrochlorothiazide
    68788-7400HydrochlorothiazideHydrochlorothiazide
    68788-9401HydrochlorothiazideHydrochlorothiazide
    68788-9920HydrochlorothiazideHydrochlorothiazide
    68788-9919HydrochlorothiazideHydrochlorothiazide
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