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Hydrochlorothiazide - Hydrochlorothiazide

Navigation: NDC > Supplier starting with: G > GREENSTONE LLC
Field Value
NDC Code: 59762-1736
Proprietary Name: Hydrochlorothiazide
Suffix:
Non-Proprietary Name: Hydrochlorothiazide
Dosage Form: TABLET
Method: ORAL
Original Marketing Date: 20-07-2007
End of Marketing: 30-06-2014
Category Name: ANDA
Application Number: ANDA040780
Labeler: GREENSTONE LLC
Substance Name: HYDROCHLOROTHIAZIDE
Active Numerator Strength: 25
Active Ingredient Unit: mg/1
Pharm Classes: Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient]
DEA Schedule: