Fosinopril Sodium

Product NDC: 0093-7222
11-digit product format: 000937222
Labeler code: 0093
Product ID: 0093-7222_8c43e05a-c30a-421f-9107-7aabe32a46af
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Fosinopril Sodium
Dosage form: TABLET
Route: ORAL
Labeler: Teva Pharmaceuticals USA, Inc.
Application: ANDA076139
Marketing category: ANDA
Marketing start: 2003-12-01
Marketing end: 2019-12-31
Substance: FOSINOPRIL SODIUM
Active strength: 10 mg/1
Pharmacologic classes: Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]
NDC exclude flag: No
Listing certified through: 0000-00-00
Current FDA listing: Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
90aa3f6a-97f0-be7e-d25b-b26d56ae287e	Product name	3	20201015

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0093-7222-10	EA - Each	0093-7222	f1f7db57-85bd-4540-9f39-7f1210ba5ff6	1	2012-07-24
0093-7222-98	EA - Each	0093-7222	6f0a4c47-6ff9-41d4-9424-818bb3588cea	1	2012-07-24

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
FOSINOPRIL SODIUM	ACTIVE INGREDIENT	NW2RTH6T2N	FOSINOPRIL SODIUM TABLET [PHYSICIANS TOTAL CARE, INC.]	2
FOSINOPRILAT	ACTIVE MOIETY	S312EY6ZT8	FOSINOPRIL SODIUM TABLET [PHYSICIANS TOTAL CARE, INC.]	2
ANHYDROUS LACTOSE	INACTIVE INGREDIENT	3SY5LH9PMK	FOSINOPRIL SODIUM TABLET [PHYSICIANS TOTAL CARE, INC.]	2
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	FOSINOPRIL SODIUM TABLET [PHYSICIANS TOTAL CARE, INC.]	2
CROSPOVIDONE	INACTIVE INGREDIENT	68401960MK	FOSINOPRIL SODIUM TABLET [PHYSICIANS TOTAL CARE, INC.]	2
GLYCERYL DIBEHENATE	INACTIVE INGREDIENT	R8WTH25YS2	FOSINOPRIL SODIUM TABLET [PHYSICIANS TOTAL CARE, INC.]	2
ISOPROPYL ALCOHOL	INACTIVE INGREDIENT	ND2M416302	FOSINOPRIL SODIUM TABLET [PHYSICIANS TOTAL CARE, INC.]	2
POVIDONE	INACTIVE INGREDIENT	FZ989GH94E	FOSINOPRIL SODIUM TABLET [PHYSICIANS TOTAL CARE, INC.]	2
SODIUM LAURYL SULFATE	INACTIVE INGREDIENT	368GB5141J	FOSINOPRIL SODIUM TABLET [PHYSICIANS TOTAL CARE, INC.]	2

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
NW2RTH6T2N	FOSINOPRIL SODIUM	88889-14-9	FOSINOPRIL SODIUM

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
857169	fosinopril sodium 10 MG Oral Tablet	PSN	e8c794ba-8a15-4e3e-ba3b-1704887628cd	2
857183	fosinopril sodium 20 MG Oral Tablet	PSN	e8c794ba-8a15-4e3e-ba3b-1704887628cd	2
857187	fosinopril sodium 40 MG Oral Tablet	PSN	e8c794ba-8a15-4e3e-ba3b-1704887628cd	2
857169	fosinopril sodium 10 MG Oral Tablet	SCD	e8c794ba-8a15-4e3e-ba3b-1704887628cd	2
857183	fosinopril sodium 20 MG Oral Tablet	SCD	e8c794ba-8a15-4e3e-ba3b-1704887628cd	2
857187	fosinopril sodium 40 MG Oral Tablet	SCD	e8c794ba-8a15-4e3e-ba3b-1704887628cd	2
857169	FNP Sodium 10 MG Oral Tablet	SY	e8c794ba-8a15-4e3e-ba3b-1704887628cd	2
857183	FNP Sodium 20 MG Oral Tablet	SY	e8c794ba-8a15-4e3e-ba3b-1704887628cd	2
857187	FNP Sodium 40 MG Oral Tablet	SY	e8c794ba-8a15-4e3e-ba3b-1704887628cd	2

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
FOSINOPRIL SODIUM TABLETS USP, 10 mg, 20 mg, and 40 mg 7222 7223 7224 Rx only	Physicians Total Care, Inc.	2013-02-05	HUMAN PRESCRIPTION DRUG LABEL	2