NDC 55289-565

Hydrochlorothiazide

Hydrochlorothiazide

Hydrochlorothiazide is a Oral Capsule, Gelatin Coated in the Human Prescription Drug category. It is labeled and distributed by Pd-rx Pharmaceuticals, In. The primary component is Hydrochlorothia.

Product ID55289-565_785e18fc-b147-6ce8-e053-2a91aa0a6d2e
NDC55289-565
Product TypeHuman Prescription Drug
Proprietary NameHydrochlorothiazide
Generic NameHydrochlorothiazide
Dosage FormCapsule, Gelatin Coated
Route of AdministrationORAL
Marketing Start Date1996-12-27
Marketing CategoryNDA AUTHORIZED / NDA AUTHORIZED GENERIC
Application NumberNDA020504
Labeler NamePD-Rx Pharmaceuticals, In
Substance NameHYDROCHLOROTHIA
Active Ingredient Strength13 mg/1
Pharm ClassesIncreased Diure
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 55289-565-07

7 CAPSULE, GELATIN COATED in 1 BOTTLE, PLASTIC (55289-565-07)
Marketing Start Date2018-03-14
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 55289-565-90 [55289056590]

Hydrochlorothiazide CAPSULE, GELATIN COATED
Marketing CategoryNDA authorized generic
Application NumberNDA020504
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2015-12-10

NDC 55289-565-14 [55289056514]

Hydrochlorothiazide CAPSULE, GELATIN COATED
Marketing CategoryNDA authorized generic
Application NumberNDA020504
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2017-05-12

NDC 55289-565-07 [55289056507]

Hydrochlorothiazide CAPSULE, GELATIN COATED
Marketing CategoryNDA authorized generic
Application NumberNDA020504
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2018-03-14

NDC 55289-565-98 [55289056598]

Hydrochlorothiazide CAPSULE, GELATIN COATED
Marketing CategoryNDA authorized generic
Application NumberNDA020504
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2015-12-10

NDC 55289-565-60 [55289056560]

Hydrochlorothiazide CAPSULE, GELATIN COATED
Marketing CategoryNDA authorized generic
Application NumberNDA020504
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2015-12-10

NDC 55289-565-30 [55289056530]

Hydrochlorothiazide CAPSULE, GELATIN COATED
Marketing CategoryNDA authorized generic
Application NumberNDA020504
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2015-12-10

Drug Details

Active Ingredients

IngredientStrength
HYDROCHLOROTHIAZIDE12.5 mg/1

Pharmacological Class

  • 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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