NDC 67253-820 - Hydrochlorothiazide

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 67253-820
Manufacturer: ReadyMeds
Effective date: 2014-06-20
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Hydrochlorothiazide - ReadyMeds	ReadyMeds	2014-06-20	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
67253-820-10	EA - Each	67253-820	4eeaf509-2063-4c62-831d-f4fd23dc0b08	1	2013-07-02
67253-820-11	EA - Each	67253-820	47684e0c-8842-4059-8b42-60bb8a561589	1	2013-07-02

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version	Uploaded
HYDROCHLOROTHIAZIDE	ACTIVE INGREDIENT	0J48LPH2TH	HYDROCHLOROTHIAZIDE TABLET [READYMEDS]	2
HYDROCHLOROTHIAZIDE	ACTIVE MOIETY	0J48LPH2TH	HYDROCHLOROTHIAZIDE TABLET [READYMEDS]	2
ANHYDROUS LACTOSE	INACTIVE INGREDIENT	3SY5LH9PMK	HYDROCHLOROTHIAZIDE TABLET [READYMEDS]	2
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	HYDROCHLOROTHIAZIDE TABLET [READYMEDS]	2
FD&C YELLOW NO. 6	INACTIVE INGREDIENT	H77VEI93A8	HYDROCHLOROTHIAZIDE TABLET [READYMEDS]	2
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	HYDROCHLOROTHIAZIDE TABLET [READYMEDS]	2
STARCH, CORN	INACTIVE INGREDIENT	O8232NY3SJ	HYDROCHLOROTHIAZIDE TABLET [READYMEDS]	2