Accupril

Product NDC: 0071-0530
11-digit product format: 000710530
Labeler code: 0071
Product ID: 0071-0530_140c689b-e8c8-4db9-9bcf-c68869e0d762
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: quinapril hydrochloride
Dosage form: TABLET, FILM COATED
Route: ORAL
Labeler: Parke-Davis Div of Pfizer Inc
Application: NDA019885
Marketing category: NDA
Marketing start: 1991-11-19
Marketing end: 0000-00-00
Substance: QUINAPRIL HYDROCHLORIDE
Active strength: 10 mg/1
Pharmacologic classes: Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA]
NDC exclude flag: No
Listing certified through: 2023-12-31
Current FDA listing: Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 3 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Source date
excluded product	product	0071-0530		D	Discontinued by firm	2026-10-16
excluded package	package	0071-0530	0071-0530-23	D	Discontinued by firm	2026-10-16
excluded package	package	0071-0530	0071-0530-40	D	Discontinued by firm	2026-10-16

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 14 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Code	Status	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	0071-0530-40	D	Discontinued by firm	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	0071-0530-40	D	Discontinued by firm	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	0071-0530-40	D	Discontinued by firm	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	0071-0530-40	D	Discontinued by firm	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	0071-0530-40	D	Discontinued by firm	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	0071-0530-40	D	Discontinued by firm	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	0071-0530-40	D	Discontinued by firm	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	0071-0530-40	D	Discontinued by firm	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	0071-0530-40	D	Discontinued by firm	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	0071-0530-23	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	0071-0530-40	D	Discontinued by firm	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	0071-0530-40	D	Discontinued by firm	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	0071-0530-40	D	Discontinued by firm	`557ba5c1ecfa…`	`9c80585c8c6e…`

Source provenance: Browse the complete Orange Book source catalog · source snapshot 44.

Orange Book products#

Current product rows page 1 of 1 · 4 matching rows.

Application-product, Trade name, Ingredient table
Application-product	Trade name	Ingredient	Strength	Dosage form / route	RLD / RS	Approval date
N019885-001	ACCUPRIL	QUINAPRIL HYDROCHLORIDE	EQ 5MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-11-19
N019885-002	ACCUPRIL	QUINAPRIL HYDROCHLORIDE	EQ 10MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-11-19
N019885-003	ACCUPRIL	QUINAPRIL HYDROCHLORIDE	EQ 20MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-11-19
N019885-004	ACCUPRIL	QUINAPRIL HYDROCHLORIDE	EQ 40MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-11-19

Observed Orange Book product history#

Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.

Product history page 1 of 5 · 176 observed states.

Captured, Edition, Application-product table
Captured	Edition	Application-product	Trade name	Strength	Dosage form / route	RLD / RS	Approval date	Source SHA-256
2026-10-15 13:18:30	2026-09	N019885-001	ACCUPRIL	EQ 5MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-11-19	`c2088c7a36db…`
2026-10-15 13:18:30	2026-09	N019885-002	ACCUPRIL	EQ 10MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-11-19	`c2088c7a36db…`
2026-10-15 13:18:30	2026-09	N019885-003	ACCUPRIL	EQ 20MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-11-19	`c2088c7a36db…`
2026-10-15 13:18:30	2026-09	N019885-004	ACCUPRIL	EQ 40MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-11-19	`c2088c7a36db…`
2026-09-14 22:38:34	2026-08	N019885-001	ACCUPRIL	EQ 5MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-11-19	`84e616aacf4f…`
2026-09-14 22:38:34	2026-08	N019885-002	ACCUPRIL	EQ 10MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-11-19	`84e616aacf4f…`
2026-09-14 22:38:34	2026-08	N019885-003	ACCUPRIL	EQ 20MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-11-19	`84e616aacf4f…`
2026-09-14 22:38:34	2026-08	N019885-004	ACCUPRIL	EQ 40MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-11-19	`84e616aacf4f…`
2026-08-18 06:07:40	2026-07	N019885-001	ACCUPRIL	EQ 5MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-11-19	`caaa826d4ba7…`
2026-08-18 06:07:40	2026-07	N019885-002	ACCUPRIL	EQ 10MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-11-19	`caaa826d4ba7…`
2026-08-18 06:07:40	2026-07	N019885-003	ACCUPRIL	EQ 20MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-11-19	`caaa826d4ba7…`
2026-08-18 06:07:40	2026-07	N019885-004	ACCUPRIL	EQ 40MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-11-19	`caaa826d4ba7…`
2026-02-19 14:30 UTC	2026-02	N019885-001	ACCUPRIL	EQ 5MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-11-19	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	N019885-002	ACCUPRIL	EQ 10MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-11-19	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	N019885-003	ACCUPRIL	EQ 20MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-11-19	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	N019885-004	ACCUPRIL	EQ 40MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-11-19	`011fe1cb6892…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N019885-001	ACCUPRIL	EQ 5MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-11-19	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N019885-002	ACCUPRIL	EQ 10MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-11-19	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N019885-003	ACCUPRIL	EQ 20MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-11-19	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N019885-004	ACCUPRIL	EQ 40MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-11-19	`31067a03dcf5…`
2025-08-23 18:47 UTC	2025-08	N019885-001	ACCUPRIL	EQ 5MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-11-19	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	N019885-002	ACCUPRIL	EQ 10MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-11-19	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	N019885-003	ACCUPRIL	EQ 20MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-11-19	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	N019885-004	ACCUPRIL	EQ 40MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-11-19	`6a471c1ec25d…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N019885-001	ACCUPRIL	EQ 5MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-11-19	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N019885-002	ACCUPRIL	EQ 10MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-11-19	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N019885-003	ACCUPRIL	EQ 20MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-11-19	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N019885-004	ACCUPRIL	EQ 40MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-11-19	`fd3edfee7708…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N019885-001	ACCUPRIL	EQ 5MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-11-19	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N019885-002	ACCUPRIL	EQ 10MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-11-19	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N019885-003	ACCUPRIL	EQ 20MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-11-19	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N019885-004	ACCUPRIL	EQ 40MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-11-19	`b8a1b40f171c…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	N019885-001	ACCUPRIL	EQ 5MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-11-19	`03ed91905a0d…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	N019885-002	ACCUPRIL	EQ 10MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-11-19	`03ed91905a0d…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	N019885-003	ACCUPRIL	EQ 20MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-11-19	`03ed91905a0d…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	N019885-004	ACCUPRIL	EQ 40MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-11-19	`03ed91905a0d…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	N019885-001	ACCUPRIL	EQ 5MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-11-19	`2680178bc6a6…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	N019885-002	ACCUPRIL	EQ 10MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-11-19	`2680178bc6a6…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	N019885-003	ACCUPRIL	EQ 20MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-11-19	`2680178bc6a6…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	N019885-004	ACCUPRIL	EQ 40MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1991-11-19	`2680178bc6a6…`

Observed Orange Book normalized TE history#

Normalized TE history page 2 of 2 · 68 observed states.

Captured, Edition, Application-product table
Captured	Edition	Application-product	TE code	Order	Source SHA-256
2019-12-14 00:12 UTC	2019-12	N019885-001	AB	1	`3f01610625f2…`
2019-12-14 00:12 UTC	2019-12	N019885-002	AB	1	`3f01610625f2…`
2019-12-14 00:12 UTC	2019-12	N019885-003	AB	1	`3f01610625f2…`
2019-12-14 00:12 UTC	2019-12	N019885-004	AB	1	`3f01610625f2…`
2019-09-15 20:21 UTC	2019-09	N019885-001	AB	1	`b00525d2431f…`
2019-09-15 20:21 UTC	2019-09	N019885-002	AB	1	`b00525d2431f…`
2019-09-15 20:21 UTC	2019-09	N019885-003	AB	1	`b00525d2431f…`
2019-09-15 20:21 UTC	2019-09	N019885-004	AB	1	`b00525d2431f…`
2019-07-19 19:46 UTC	2019-07	N019885-001	AB	1	`ea99ee380514…`
2019-07-19 19:46 UTC	2019-07	N019885-002	AB	1	`ea99ee380514…`
2019-07-19 19:46 UTC	2019-07	N019885-003	AB	1	`ea99ee380514…`
2019-07-19 19:46 UTC	2019-07	N019885-004	AB	1	`ea99ee380514…`
2022-11-12 20:34 UTC · 5 captures of this ZIP	2022-11	N019885-001	AB	1	`3a93d1ddd44b…`
2022-11-12 20:34 UTC · 5 captures of this ZIP	2022-11	N019885-002	AB	1	`3a93d1ddd44b…`
2022-11-12 20:34 UTC · 5 captures of this ZIP	2022-11	N019885-003	AB	1	`3a93d1ddd44b…`
2022-11-12 20:34 UTC · 5 captures of this ZIP	2022-11	N019885-004	AB	1	`3a93d1ddd44b…`
2022-10-28 04:53 UTC	2022-10	N019885-001	AB	1	`f41ea6bd6efb…`
2022-10-28 04:53 UTC	2022-10	N019885-002	AB	1	`f41ea6bd6efb…`
2022-10-28 04:53 UTC	2022-10	N019885-003	AB	1	`f41ea6bd6efb…`
2022-10-28 04:53 UTC	2022-10	N019885-004	AB	1	`f41ea6bd6efb…`
2022-09-29 23:25 UTC	2022-09	N019885-001	AB	1	`e64feba35796…`
2022-09-29 23:25 UTC	2022-09	N019885-002	AB	1	`e64feba35796…`
2022-09-29 23:25 UTC	2022-09	N019885-003	AB	1	`e64feba35796…`
2022-09-29 23:25 UTC	2022-09	N019885-004	AB	1	`e64feba35796…`
2022-07-09 03:26 UTC · 3 captures of this ZIP	2022-07	N019885-001	AB	1	`cb3db0bc1861…`
2022-07-09 03:26 UTC · 3 captures of this ZIP	2022-07	N019885-002	AB	1	`cb3db0bc1861…`
2022-07-09 03:26 UTC · 3 captures of this ZIP	2022-07	N019885-003	AB	1	`cb3db0bc1861…`
2022-07-09 03:26 UTC · 3 captures of this ZIP	2022-07	N019885-004	AB	1	`cb3db0bc1861…`

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0071-0530-23	EA - Each	0071-0530	f8f23f0b-c24a-4624-a34a-cea252ae5de5	1	2012-07-24
0071-0530-40	EA - Each	0071-0530	6012bf51-a9f3-4956-89fc-c57cb89dec0e	1	2012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
QUINAPRIL HYDROCHLORIDE	ACTIVE INGREDIENT	33067B3N2M	ACCUPRIL (QUINAPRIL HYDROCHLORIDE) TABLET, FILM COATED [PARKE-DAVIS DIV OF PFIZER INC]	13
QUINAPRILAT	ACTIVE MOIETY	34SSX5LDE5	ACCUPRIL (QUINAPRIL HYDROCHLORIDE) TABLET, FILM COATED [PARKE-DAVIS DIV OF PFIZER INC]	13
CANDELILLA WAX	INACTIVE INGREDIENT	WL0328HX19	ACCUPRIL (QUINAPRIL HYDROCHLORIDE) TABLET, FILM COATED [PARKE-DAVIS DIV OF PFIZER INC]	13
CROSPOVIDONE	INACTIVE INGREDIENT	68401960MK	ACCUPRIL (QUINAPRIL HYDROCHLORIDE) TABLET, FILM COATED [PARKE-DAVIS DIV OF PFIZER INC]	13
FERRIC OXIDE RED	INACTIVE INGREDIENT	1K09F3G675	ACCUPRIL (QUINAPRIL HYDROCHLORIDE) TABLET, FILM COATED [PARKE-DAVIS DIV OF PFIZER INC]	13
GELATIN	INACTIVE INGREDIENT	2G86QN327L	ACCUPRIL (QUINAPRIL HYDROCHLORIDE) TABLET, FILM COATED [PARKE-DAVIS DIV OF PFIZER INC]	13
LACTOSE	INACTIVE INGREDIENT	J2B2A4N98G	ACCUPRIL (QUINAPRIL HYDROCHLORIDE) TABLET, FILM COATED [PARKE-DAVIS DIV OF PFIZER INC]	13
MAGNESIUM CARBONATE	INACTIVE INGREDIENT	0E53J927NA	ACCUPRIL (QUINAPRIL HYDROCHLORIDE) TABLET, FILM COATED [PARKE-DAVIS DIV OF PFIZER INC]	13
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	ACCUPRIL (QUINAPRIL HYDROCHLORIDE) TABLET, FILM COATED [PARKE-DAVIS DIV OF PFIZER INC]	13
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	ACCUPRIL (QUINAPRIL HYDROCHLORIDE) TABLET, FILM COATED [PARKE-DAVIS DIV OF PFIZER INC]	13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0071-0530	ACCUPRIL (QUINAPRIL HYDROCHLORIDE) TABLET, FILM COATED ACCUPRIL (QUINAPRIL) TABLET, FILM COATED [PARKE-DAVIS DIV OF PFIZER INC]	26	Legacy NDC	20250119_63cf5651-d52c-4d27-9fd4-ed9cd9724dff.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
33067B3N2M	QUINAPRIL HYDROCHLORIDE	82586-55-8	QUINAPRIL HYDROCHLORIDE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
0071-0530-23	00071053023	90 TABLET, FILM COATED in 1 BOTTLE (0071-0530-23)		1991-11-19	0000-00-00	No	No	Current
0071-0530-40	00071053040	100 BLISTER PACK in 1 CARTON (0071-0530-40) > 1 TABLET, FILM COATED in 1 BLISTER PACK	100 blister pack	1991-11-19	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Accupril ® (quinapril) Tablets	Parke-Davis Div of Pfizer Inc \| Pfizer Inc	2025-01-16	HUMAN PRESCRIPTION DRUG LABEL	26