Lovastatin

Product NDC: 50090-0757
Requested package NDC: 50090-0757-1
11-digit product format: 500900757
Labeler code: 50090
Product ID: 50090-0757_80023785-4b99-48c1-b757-c391056fe6fc
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Lovastatin
Dosage form: TABLET
Route: ORAL
Labeler: A-S Medication Solutions
Application: ANDA075991
Marketing category: ANDA
Marketing start: 2002-11-25
Substance: LOVASTATIN
Active strength: 10 mg/1
Pharmacologic classes: HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

NDC auxiliary status#

Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.

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

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	50090-0757	50090-0757-1	D	Discontinued by firm		2026-07-31

Source provenance: Browse the complete Orange Book source catalog · source snapshot 1.

Orange Book products#

Current product rows page 1 of 1 · 3 matching rows.

Application-product, Trade name, Ingredient table
Application-product	Trade name	Ingredient	Strength	Dosage form / route	TE codes	RLD / RS	Approval date
A075991-001	LOVASTATIN	LOVASTATIN	10MG	TABLET / ORAL	AB		2002-06-05
A075991-002	LOVASTATIN	LOVASTATIN	20MG	TABLET / ORAL	AB		2002-06-05
A075991-003	LOVASTATIN	LOVASTATIN	40MG	TABLET / ORAL	AB	RS	2002-06-05

Therapeutic equivalence codes#

Current TE-code rows page 1 of 1 · 3 matching rows.

Application-product, TE code table
Application-product	TE code
A075991-001	AB
A075991-002	AB
A075991-003	AB

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.

Captured, Edition, Application-product table
Captured	Edition	Application-product	Trade name	Strength	Dosage form / route	Product TE source text	RLD / RS	Approval date	Source SHA-256
2026-08-01 22:54:32	2026-06	A075991-001	LOVASTATIN	10MG	TABLET / ORAL	AB		2002-06-05	`a50c72e98297…`
2026-08-01 22:54:32	2026-06	A075991-002	LOVASTATIN	20MG	TABLET / ORAL	AB		2002-06-05	`a50c72e98297…`
2026-08-01 22:54:32	2026-06	A075991-003	LOVASTATIN	40MG	TABLET / ORAL	AB	RS	2002-06-05	`a50c72e98297…`

Observed Orange Book normalized TE history#

Captured, Edition, Application-product table
Captured	Edition	Application-product	TE code	Order	Source SHA-256
2026-08-01 22:54:32	2026-06	A075991-001	AB	1	`a50c72e98297…`
2026-08-01 22:54:32	2026-06	A075991-002	AB	1	`a50c72e98297…`
2026-08-01 22:54:32	2026-06	A075991-003	AB	1	`a50c72e98297…`

openFDA label cross-check#

Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.

Matched openFDA labels page 1 of 2 · 28 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Lovastatin	LOVASTATIN	REMEDYREPACK INC.	9438d8a0-ca5b-4676-aab9-d0241ccff6c9	2026-07-23	Warnings, Adverse reactions	Exact identifier application applno (ANDA): 075991 application number: ANDA075991
Lovastatin	LOVASTATIN	Preferred Pharmaceuticals Inc.	56680dfa-abe6-4587-b222-364315fd78f4	2026-06-03	Warnings, Adverse reactions	Exact identifier application applno (ANDA): 075991 application number: ANDA075991
Lovastatin	LOVASTATIN	Preferred Pharmaceuticals, Inc.	ea4df37b-21e9-4dc3-83af-1be1b50bfdc9	2026-06-03	Warnings, Adverse reactions	Exact identifier application applno (ANDA): 075991 application number: ANDA075991
Lovastatin	LOVASTATIN	Bryant Ranch Prepack	7fd9d5c7-8025-4049-8b5b-ae3d22db507f	2026-03-09	Warnings, Adverse reactions	Exact identifier application applno (ANDA): 075991 application number: ANDA075991
Lovastatin	LOVASTATIN	Northwind Health Company, LLC	db47ddae-c574-427f-e053-2a95a90aae48	2026-01-01	Warnings, Adverse reactions	Exact identifier application applno (ANDA): 075991 application number: ANDA075991
Lovastatin	LOVASTATIN	A-S Medication Solutions	dd7a223e-7fc5-4eb0-9bd7-2f9a2d6b4173	2025-10-10	Warnings, Adverse reactions	Exact identifier application applno (ANDA): 075991 application number: ANDA075991
Lovastatin	LOVASTATIN	A-S Medication Solutions	bfb889a4-5751-4706-9fa7-f48672c1bc08	2025-10-10	Warnings, Adverse reactions	Exact identifier application applno (ANDA): 075991 application number: ANDA075991
Lovastatin	LOVASTATIN	Bryant Ranch Prepack	220a9b3c-c583-49e3-8bf0-d0c97dc9b829	2025-04-01	Warnings, Adverse reactions	Exact identifier application applno (ANDA): 075991 application number: ANDA075991
Lovastatin	LOVASTATIN	PD-Rx Pharmaceuticals, Inc.	c37206ae-52f1-4192-9ab9-3044247cf58d	2025-03-13	Warnings, Adverse reactions	Exact identifier application applno (ANDA): 075991 application number: ANDA075991
Lovastatin	LOVASTATIN	PD-Rx Pharmaceuticals, Inc.	ac86821f-d741-4ab1-bd03-ce8797dd4f34	2025-03-12	Warnings, Adverse reactions	Exact identifier application applno (ANDA): 075991 application number: ANDA075991
Lovastatin	LOVASTATIN	PD-Rx Pharmaceuticals, Inc.	70e2bf86-4a78-4dfb-b6b1-8eb95f63684d	2025-03-06	Warnings, Adverse reactions	Exact identifier application applno (ANDA): 075991 application number: ANDA075991
Lovastatin	LOVASTATIN	PD-Rx Pharmaceuticals, Inc.	eea93a4b-f804-4b9c-aabf-e906f03c1e80	2025-02-28	Warnings, Adverse reactions	Exact identifier application applno (ANDA): 075991 application number: ANDA075991
Lovastatin	LOVASTATIN	Boswell Pharmacy Services LLC d/b/a BPS Wholesale	2eff3e5e-8746-048e-e063-6294a90a38c4	2025-02-25	Warnings, Adverse reactions	Exact identifier application applno (ANDA): 075991 application number: ANDA075991
Lovastatin	LOVASTATIN	Carlsbad Technology, Inc.	0a680e13-0356-4e08-a7fe-78b96ba51b9d	2025-01-07	Warnings, Adverse reactions	Exact identifier application applno (ANDA): 075991 application number: ANDA075991
Lovastatin	LOVASTATIN	Bryant Ranch Prepack	c871a6a7-67a4-4ac1-b102-3f1604625c7d	2024-09-12	Warnings, Adverse reactions	Exact identifier application applno (ANDA): 075991 application number: ANDA075991
Lovastatin	LOVASTATIN	NuCare Pharmaceuticals, Inc.	415c2698-7787-49f8-e054-00144ff88e88	2024-08-14	Warnings, Adverse reactions	Exact identifier application applno (ANDA): 075991 application number: ANDA075991
Lovastatin	LOVASTATIN	NuCare Pharmaceuticals, Inc.	4444573e-9df1-01e6-e054-00144ff8d46c	2024-08-14	Warnings, Adverse reactions	Exact identifier application applno (ANDA): 075991 application number: ANDA075991
Lovastatin	LOVASTATIN	Bryant Ranch Prepack	8d8199ca-df39-4eb8-a905-dee3ab7e2973	2024-08-14	Warnings, Adverse reactions	Exact identifier application applno (ANDA): 075991 application number: ANDA075991
Lovastatin	LOVASTATIN	Bryant Ranch Prepack	5684ceb8-a5b2-4fb4-92be-14aabcea3871	2024-08-09	Warnings, Adverse reactions	Exact identifier application applno (ANDA): 075991 application number: ANDA075991
Lovastatin	LOVASTATIN	Bryant Ranch Prepack	ad905651-6e3a-4140-aa37-d91e5f37c0f0	2024-08-08	Warnings, Adverse reactions	Exact identifier application applno (ANDA): 075991 application number: ANDA075991

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
dc9a5fb6-14e2-1cc8-a567-a781fd1f0212	Product name	1	20140508
f1ae760e-e8ec-b0b4-fb1b-2db7c49fcec5	Product name	1	20140508
fecc3d5d-ff9a-60ad-1a3a-6cb9b21df758	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
50090-0757-0	2023-02-07	C162847	48780-1	f386c64a-3248-0266-e053-dadaa90a7c1a	Lovastatin Tablet USP Revision M
50090-0757-1	2023-02-07	C162847	48780-1	f386c64a-3248-0266-e053-dadaa90a7c1a	Lovastatin Tablet USP Revision M
50090-0757-0	2023-01-30	C162847	48780-1	f386c64a-3248-0266-e053-dadaa90a7c1a	Lovastatin Tablet USP Revision M
50090-0757-1	2023-01-30	C162847	48780-1	f386c64a-3248-0266-e053-dadaa90a7c1a	Lovastatin Tablet USP Revision M

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
50090-0757-0	Lovastatin	30 in 1 BOTTLE	TABLET	30		20
50090-0757-1	Lovastatin	90 in 1 BOTTLE	TABLET	90		20

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
50090-0757-0	EA - Each	50090-0757	9e257e17-ff01-4aa3-8c23-cd956dbde9ae	1	2021-08-05
50090-0757-1	EA - Each	50090-0757	31adccd9-9889-4c37-a80c-7424aff85ef4	1	2021-08-05

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
50090-0757	LOVASTATIN TABLET [A-S MEDICATION SOLUTIONS]	20	Current NDC, Legacy NDC, 2 package rows	20230208_5e4555fe-c73c-44ff-973a-a5fd24122830.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
9LHU78OQFD	LOVASTATIN	75330-75-5	LOVASTATIN

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
50090-0757-1	50090075701	90 TABLET in 1 BOTTLE (50090-0757-1)	90 tablet	2014-11-28	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Lovastatin Tablet USP Revision M	A-S Medication Solutions	2023-02-04	HUMAN PRESCRIPTION DRUG LABEL	20