NDC 67046-277

Hydrochlorothiazide

Hydrochlorothiazide

Hydrochlorothiazide is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Contract Pharmacy Services-pa. The primary component is Hydrochlorothiazide.

Product ID67046-277_5a40e342-6004-a20c-e053-2a91aa0a472e
NDC67046-277
Product TypeHuman Prescription Drug
Proprietary NameHydrochlorothiazide
Generic NameHydrochlorothiazide
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2017-09-28
Marketing CategoryANDA / ANDA
Application NumberANDA040807
Labeler NameContract Pharmacy Services-PA
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 67046-277-07

7 TABLET in 1 BLISTER PACK (67046-277-07)
Marketing Start Date2017-09-28
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 67046-277-21 [67046027721]

Hydrochlorothiazide TABLET
Marketing CategoryANDA
Application NumberANDA040807
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-28

NDC 67046-277-15 [67046027715]

Hydrochlorothiazide TABLET
Marketing CategoryANDA
Application NumberANDA040807
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-28

NDC 67046-277-28 [67046027728]

Hydrochlorothiazide TABLET
Marketing CategoryANDA
Application NumberANDA040807
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-28

NDC 67046-277-30 [67046027730]

Hydrochlorothiazide TABLET
Marketing CategoryANDA
Application NumberANDA040807
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-28

NDC 67046-277-07 [67046027707]

Hydrochlorothiazide TABLET
Marketing CategoryANDA
Application NumberANDA040807
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-28

NDC 67046-277-20 [67046027720]

Hydrochlorothiazide TABLET
Marketing CategoryANDA
Application NumberANDA040807
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-28

NDC 67046-277-14 [67046027714]

Hydrochlorothiazide TABLET
Marketing CategoryANDA
Application NumberANDA040807
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-28

NDC 67046-277-60 [67046027760]

Hydrochlorothiazide TABLET
Marketing CategoryANDA
Application NumberANDA040807
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-28

Drug Details

Active Ingredients

IngredientStrength
HYDROCHLOROTHIAZIDE25 mg/1

OpenFDA Data

SPL SET ID:5a40e342-6003-a20c-e053-2a91aa0a472e
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 310798
    • UPC Code
  • 0323155047103

    • Pharmacological Class

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

    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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