Fosinopril Sodium and Hydrochlorothiazide

Product NDC: 63629-6993
11-digit product format: 636296993
Labeler code: 63629
Product ID: 63629-6993_2c585e38-3944-48bc-9a4f-a1da892a9342
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Fosinopril Sodium and Hydrochlorothiazide
Dosage form: TABLET
Route: ORAL
Labeler: Bryant Ranch Prepack
Application: ANDA079245
Marketing category: ANDA
Marketing start: 2009-07-09
Marketing end: 0000-00-00
Substance: FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE
Active strength: 10 mg/1; mg/1
Pharmacologic classes: Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]
NDC exclude flag: No
Listing certified through: 2021-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
63629-6993-1	2020-10-16	C162847	48780-1	9d75b9d0-830e-f424-e053-dadaa90a57ce	ebbddf45-1664-4815-bf26-1639a26bc894
63629-6993-1	2020-01-31	C162847	48780-1	9d75b9d0-830e-f424-e053-dadaa90a57ce	ebbddf45-1664-4815-bf26-1639a26bc894

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
NW2RTH6T2N	FOSINOPRIL SODIUM	88889-14-9	FOSINOPRIL SODIUM
0J48LPH2TH	HYDROCHLOROTHIAZIDE	58-93-5	HYDROCHLOROTHIAZIDE

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
63629-6993-1	63629699301	30 TABLET in 1 BOTTLE (63629-6993-1)	30 tablet	2016-04-29	0000-00-00	No	No	Current