NDC 71335-1350

Hydrochlorothiazide

Hydrochlorothiazide

Hydrochlorothiazide is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Hydrochlorothiazide.

Product ID71335-1350_0266d5b9-5f7a-44b1-af82-eed48414939f
NDC71335-1350
Product TypeHuman Prescription Drug
Proprietary NameHydrochlorothiazide
Generic NameHydrochlorothiazide
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date1973-01-12
Marketing CategoryANDA / ANDA
Application NumberANDA083177
Labeler NameBryant Ranch Prepack
Substance NameHYDROCHLOROTHIAZIDE
Active Ingredient Strength25 mg/1
Pharm ClassesIncreased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 71335-1350-0

120 TABLET in 1 BOTTLE (71335-1350-0)
Marketing Start Date2021-12-28
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71335-1350-8 [71335135008]

Hydrochlorothiazide TABLET
Marketing CategoryANDA
Application NumberANDA083177
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1973-01-12

NDC 71335-1350-0 [71335135000]

Hydrochlorothiazide TABLET
Marketing CategoryANDA
Application NumberANDA083177
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1973-01-12

NDC 71335-1350-9 [71335135009]

Hydrochlorothiazide TABLET
Marketing CategoryANDA
Application NumberANDA083177
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1973-01-12

NDC 71335-1350-6 [71335135006]

Hydrochlorothiazide TABLET
Marketing CategoryANDA
Application NumberANDA083177
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1973-01-12

NDC 71335-1350-2 [71335135002]

Hydrochlorothiazide TABLET
Marketing CategoryANDA
Application NumberANDA083177
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1973-01-12

NDC 71335-1350-7 [71335135007]

Hydrochlorothiazide TABLET
Marketing CategoryANDA
Application NumberANDA083177
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1973-01-12

NDC 71335-1350-5 [71335135005]

Hydrochlorothiazide TABLET
Marketing CategoryANDA
Application NumberANDA083177
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1973-01-12

NDC 71335-1350-4 [71335135004]

Hydrochlorothiazide TABLET
Marketing CategoryANDA
Application NumberANDA083177
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1973-01-12

NDC 71335-1350-1 [71335135001]

Hydrochlorothiazide TABLET
Marketing CategoryANDA
Application NumberANDA083177
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1973-01-12

NDC 71335-1350-3 [71335135003]

Hydrochlorothiazide TABLET
Marketing CategoryANDA
Application NumberANDA083177
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1973-01-12

Drug Details

Active Ingredients

IngredientStrength
HYDROCHLOROTHIAZIDE25 mg/1

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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