NDC 70518-3182-01 - Finasteride

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: 70518-3182
Requested NDC: 70518-3182-01
Package NDCs from labels: 70518-3182-1, 70518-3182-0, 70518-3182-3, 70518-3182-2, 70518-3182-01
Manufacturer: REMEDYREPACK INC.
Effective date: 2026-10-09
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Finasteride - REMEDYREPACK INC.	REMEDYREPACK INC.	2026-10-09	HUMAN PRESCRIPTION DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

Effective, Related label table
Effective	Related label
2023-03-20	These highlights do not include all the information needed to use finasteride tablets USP safely and effectively. See full prescribing information for finasteride tablets USP. FINASTERIDE Tablets USP, 5 mg for oral use Initial U.S. Approval: 1992
2023-03-20	These highlights do not include all the information needed to use finasteride tablets USP safely and effectively. See full prescribing information for finasteride tablets USP. FINASTERIDE Tablets USP, 5 mg for oral use Initial U.S. Approval: 1992
2023-01-30	These highlights do not include all the information needed to use finasteride tablets USP safely and effectively. See full prescribing information for finasteride tablets USP. FINASTERIDE Tablets USP, 5 mg for oral use Initial U.S. Approval: 1992
2023-01-30	These highlights do not include all the information needed to use finasteride tablets USP safely and effectively. See full prescribing information for finasteride tablets USP. FINASTERIDE Tablets USP, 5 mg for oral use Initial U.S. Approval: 1992

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
70518-3182-0	Finasteride	30 in 1 BOX	TABLET, FILM COATED	30	8
70518-3182-1	Finasteride	1 in 1 POUCH	TABLET, FILM COATED	1	8
70518-3182-2	Finasteride	30 in 1 BOX	TABLET, FILM COATED	30	8
70518-3182-3	Finasteride	1 in 1 POUCH	TABLET, FILM COATED	1	8

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
70518-3182	FINASTERIDE TABLET, FILM COATED [REMEDYREPACK INC.]	5	Current NDC, Legacy NDC, 4 package rows	20241013_c2875bc7-e811-4860-9131-da06cecc2137.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 83 of 121 · 2,408 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Light Illusion Luminous Makeup Nude-Skin Feel SPF18 MOCHA	OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE	COSMAX USA, INC	29aba80c-55b7-b8d9-e063-6294a90a5cc1	2024-12-19	Warnings	Exact identifier unii: 15FIX9V2JP
Light Illusion Luminous Makeup Nude-Skin Feel SPF18 COCOA	OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE	COSMAX USA, INC	29abe97b-e9b3-6e27-e063-6294a90ae3ed	2024-12-19	Warnings	Exact identifier unii: 15FIX9V2JP
Light Illusion Luminous Makeup Nude-Skin Feel SPF18 DEEP GOLDEN	OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE	COSMAX USA, INC	29abdf3c-fb54-a5e3-e063-6394a90af450	2024-12-19	Warnings	Exact identifier unii: 15FIX9V2JP
CeraVe Developed with Dermatologists Hydrating Mineral Sunscreen Broad Spectrum SPF 30 Face Sheer Tint Sunscreen	TITANIUM DIOXIDE AND ZINC OXIDE	L'Oreal USA Products, Inc.	f2e34230-7bfb-455f-8b33-6bff96fd9f0a	2024-12-19	Warnings	Exact identifier unii: 15FIX9V2JP
Stimulant Laxative Plus Stool Softener	DOCUSATE SODIUM 50 MG AND SENNOSIDES 8.6 MG	RUGBY LABORATORIES	f5afd8eb-d35d-44ab-897d-1d41c98ca138	2024-12-19	Warnings	Exact identifier unii: F05Q2T2JA0
Senexon-S	DOCUSATE SODIUM 50MG AND SENNOSIDES 8.6MG	RUGBY LABORATORIES	2e758ff1-3083-4245-8f58-1c47b042bfdd	2024-12-19	Warnings	Exact identifier unii: F05Q2T2JA0
Finasteride	FINASTERIDE	Dr. Reddy's Laboratories Limited	fa19372d-027d-a91b-f58e-1bdb8fd7e2b6	2024-12-19	Warnings, Adverse reactions	Exact identifier unii: 57GNO57U7G
Quality Choice Stool Softener	DOCUSATE SODIUM	Chain Drug Marketing Association	4d5facd4-f57f-44f7-b8dd-83a33e57afd9	2024-12-18	Warnings	Exact identifier unii: F05Q2T2JA0
Light Illusion Luminous Makeup Nude-Skin Feel SPF18 SHELL	OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE	COSMAX USA, INC	29868d60-b900-e0ad-e063-6294a90af87a	2024-12-18	Warnings	Exact identifier unii: 15FIX9V2JP
Belasol Suncream Non Tinted Moisturizing Sunscreen SPF 50 Jasmine	TITANIUM DIOXIDE, ZINC OXIDE	EK Clothing LLC dba Belasol	e999d752-6c00-459e-b6c3-d264c330597d	2024-12-18	Warnings	Exact identifier unii: 15FIX9V2JP
Belasol Suncream Non Tinted Moisturizing Sunscreen SPF 50	TITANIUM DIOXIDE, ZINC OXIDE	EK Clothing LLC dba Belasol	f22626c1-0996-41d8-a2ec-3bf7491df657	2024-12-18	Warnings	Exact identifier unii: 15FIX9V2JP
Good Neighbor Stool Softener	DOCUSATE SODIUM	AmerisourceBergen Drug Corp	88d657a1-77be-412a-9295-034872db2dde	2024-12-18	Warnings	Exact identifier unii: F05Q2T2JA0
Preferred Stool Softener	DOCUSATE SODIUM	Reese Pharmaceutical Co	217d13a0-3205-492c-af49-82eb80dba53a	2024-12-18	Warnings	Exact identifier unii: F05Q2T2JA0
Topcare Stool Softener	DOCUSATE SODIUM	TOPCO ASSOCIATES LLC	9342c1b5-5d35-4b60-b347-c208c0774cdc	2024-12-18	Warnings	Exact identifier unii: F05Q2T2JA0
HEB Stool Softener	DOCUSATE SODIUM	H E B	3a513cb9-8404-43dc-a780-040bf9f1741d	2024-12-18	Warnings	Exact identifier unii: F05Q2T2JA0
Topcare Stool Softener laxative	DOCUSATE SODIUM	TOPCO ASSOCIATES LLC	f9302fc2-684d-4cc2-bdd7-7ad0e9304edb	2024-12-18	Warnings	Exact identifier unii: F05Q2T2JA0
Good Neighbor Stool Softener laxative	DOCUSATE SODIUM	AmerisourceBergen Drug Corp	d09151ae-1cc6-4e69-8d80-7813082a4236	2024-12-18	Warnings	Exact identifier unii: F05Q2T2JA0
Winco Stool Softener	DOCUSATE SODIUM	WinCo Foods, LLC	4de2e315-5ec6-4ddf-8617-4e07ba456354	2024-12-18	Warnings	Exact identifier unii: F05Q2T2JA0
H E B Stool Softener laxative	DOCUSATE SODIUM	H E B	9d848fdd-3a2f-45c6-9ff3-17f1d74e0f4f	2024-12-18	Warnings	Exact identifier unii: F05Q2T2JA0
SPF 50 plus Sunscreen All Mineral Active Ingredients	TITANIUM DIOXIDE AND ZINC OXIDE	KAS Direct LLC dba BabyGanics	247aae3d-1845-4dd8-b774-b9e8214809a2	2024-12-18	Warnings	Exact identifier unii: 15FIX9V2JP

Reported adverse events (FAERS/openFDA)#

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