NDC 60505-0102-01 - Etodolac

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: 60505-0102
Requested NDC: 60505-0102-01
Package NDCs from labels: 60505-0102-1, 60505-0102-2, 60505-0102-01
Manufacturer: REMEDYREPACK INC.
Effective date: 2026-10-20
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
ETODOLAC TABLETS, USP 400 mg and 500 mg Rx only	REMEDYREPACK INC.	2026-10-20	HUMAN PRESCRIPTION DRUG LABEL
ETODOLAC TABLETS, USP 400 mg and 500 mg Rx only	Apotex Corp. \| Apotex Inc.	2026-09-11	HUMAN PRESCRIPTION DRUG LABEL
ETODOLAC TABLETS, USP 500 mg Rx only	PD-Rx Pharmaceuticals, Inc.	2026-05-05	HUMAN PRESCRIPTION DRUG LABEL
Etodolac - Bryant Ranch Prepack	Bryant Ranch Prepack	2024-09-05	HUMAN PRESCRIPTION DRUG LABEL
ETODOLAC TABLETS, USP 400 mg and 500 mg Rx only	Medsource Pharmaceuticals \| Apotex Inc.	2024-03-05	HUMAN PRESCRIPTION DRUG LABEL
Etodolac - A-S Medication Solutions	A-S Medication Solutions	2023-12-10	HUMAN PRESCRIPTION DRUG LABEL
Etodolac - Proficient Rx LP	Proficient Rx LP	2022-11-01	HUMAN PRESCRIPTION DRUG LABEL
Etodolac - Quality Care Products, LLC	Quality Care Products, LLC	2022-08-01	HUMAN PRESCRIPTION DRUG LABEL
ETODOLAC - DIRECT RX	DIRECT RX	2020-01-20	HUMAN PRESCRIPTION DRUG LABEL
ETODOLAC TABLETS, USP 400 mg and 500 mg Rx only	Preferred Pharmaceuticals Inc.	2019-09-16	HUMAN PRESCRIPTION DRUG LABEL
ETODOLAC - DIRECT RX	DIRECT RX	2019-04-30	HUMAN PRESCRIPTION DRUG LABEL
Etodolac - Aidarex Pharmaceuticals LLC \| Aidarex Pharmaceuticals	Aidarex Pharmaceuticals LLC \| Aidarex Pharmaceuticals	2018-08-21	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
60505-0102-1	Etodolac	100 in 1 BOTTLE	TABLET, FILM COATED	100		16
60505-0102-2	Etodolac	500 in 1 BOTTLE	TABLET, FILM COATED	500		16

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
60505-0102	ETODOLAC TABLET, FILM COATED [APOTEX CORP.]	15	Current NDC, Legacy NDC, 2 package rows	20240809_4d682f98-1e8a-4c2b-6df3-169d2ed10dc1.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
60505-0102-1	EA - Each	60505-0102	4b45057f-ad61-4cd5-9d3c-dbc1ec0f2c10	1	2012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
ETODOLAC	ACTIVE INGREDIENT	2M36281008	ETODOLAC TABLET, FILM COATED [APOTEX CORP.]	5
ETODOLAC	ACTIVE MOIETY	2M36281008	ETODOLAC TABLET, FILM COATED [APOTEX CORP.]	5
CROSPOVIDONE	INACTIVE INGREDIENT	68401960MK	ETODOLAC TABLET, FILM COATED [APOTEX CORP.]	5
HYDROXYPROPYL CELLULOSE (TYPE H)	INACTIVE INGREDIENT	RFW2ET671P	ETODOLAC TABLET, FILM COATED [APOTEX CORP.]	5
HYPROMELLOSE 2208 (100 MPA.S)	INACTIVE INGREDIENT	B1QE5P712K	ETODOLAC TABLET, FILM COATED [APOTEX CORP.]	5
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	ETODOLAC TABLET, FILM COATED [APOTEX CORP.]	5
METHYLCELLULOSE (100 CPS)	INACTIVE INGREDIENT	4GFU244C4J	ETODOLAC TABLET, FILM COATED [APOTEX CORP.]	5
POLYETHYLENE GLYCOL 1500	INACTIVE INGREDIENT	1212Z7S33A	ETODOLAC TABLET, FILM COATED [APOTEX CORP.]	5
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	ETODOLAC TABLET, FILM COATED [APOTEX CORP.]	5
ETODOLAC	ACTIVE INGREDIENT	2M36281008	ETODOLAC TABLET, FILM COATED [DIRECT RX]	1
ETODOLAC	ACTIVE MOIETY	2M36281008	ETODOLAC TABLET, FILM COATED [DIRECT RX]	1
Cellulose, Microcrystalline	INACTIVE INGREDIENT	OP1R32D61U	ETODOLAC TABLET, FILM COATED [DIRECT RX]	1
Ferric Oxide Red	INACTIVE INGREDIENT	1K09F3G675	ETODOLAC TABLET, FILM COATED [DIRECT RX]	1
Ferric Oxide Yellow	INACTIVE INGREDIENT	EX438O2MRT	ETODOLAC TABLET, FILM COATED [DIRECT RX]	1
Hypromelloses	INACTIVE INGREDIENT	3NXW29V3WO	ETODOLAC TABLET, FILM COATED [DIRECT RX]	1
Lactose Monohydrate	INACTIVE INGREDIENT	EWQ57Q8I5X	ETODOLAC TABLET, FILM COATED [DIRECT RX]	1
Magnesium Stearate	INACTIVE INGREDIENT	70097M6I30	ETODOLAC TABLET, FILM COATED [DIRECT RX]	1
Polyethylene Glycols	INACTIVE INGREDIENT	3WJQ0SDW1A	ETODOLAC TABLET, FILM COATED [DIRECT RX]	1
Povidone	INACTIVE INGREDIENT	FZ989GH94E	ETODOLAC TABLET, FILM COATED [DIRECT RX]	1
Sodium Starch Glycolate Type A Potato	INACTIVE INGREDIENT	5856J3G2A2	ETODOLAC TABLET, FILM COATED [DIRECT RX]	1
Titanium Dioxide	INACTIVE INGREDIENT	15FIX9V2JP	ETODOLAC TABLET, FILM COATED [DIRECT RX]	1

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 68 of 111 · 2,208 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
REPAIRWEAR UPLIFTING FIRMING BROAD SPECTRUM SPF 15 DRY	OCTINOXATE, OCTISALATE, AND TITANIUM DIOXIDE	CLINIQUE LABORATORIES LLC	07701e11-8a7e-44c5-b46e-5b48264eacad	2025-04-14	Warnings	Exact identifier unii: 15FIX9V2JP
Smoothing Mineral Sunscreen Tinted	TITANIUM DIOXIDE, ZINC OXIDE	DANIEL BEHROOZAN MD A MEDICAL CORPORATION	327246c2-9d7a-2d34-e063-6294a90a5fb7	2025-04-10		Exact identifier unii: 15FIX9V2JP
Clarity Rx Physical Skin Defense SPF 50	ZINC OXIDE AND TITANIUM DIOXIDE	Topiderm, Inc.	b5111012-97b9-4908-95a0-d09595f9c4d9	2025-04-10	Warnings	Exact identifier unii: 15FIX9V2JP
Tinted Mineral Sunscreen SPF 50	ZINC OXIDE AND TITANIUM DIOXIDE	Topiderm, Inc.	13e5085f-df2b-46b2-b063-e58ce4379905	2025-04-09	Warnings	Exact identifier unii: 15FIX9V2JP
a4723d3e-ed23-482e-a8c6-eab58f38cce4			76f5172a-9fd8-40f8-b699-cb9b1d05a614	2025-04-08	Boxed warning, Warnings, Adverse reactions	Exact identifier spl set id: 76f5172a-9fd8-40f8-b699-cb9b1d05a614
ALEX MD PHD Sheer Mineral Sunscreen	ZINC OXIDE, TITANIUM DIOXIDE	PHYSICIAN LABORATORIES INC	8f64c4fa-92ee-4af0-ab1b-6c3673f9a622	2025-03-28	Warnings	Exact identifier unii: 15FIX9V2JP
ALEX MD PHD Tinted Mineral Sunscreen	ZINC OXIDE, TITANIUM DIOXIDE	PHYSICIAN LABORATORIES INC	93873c34-5c72-43c8-b6c2-c65b596191d7	2025-03-28	Warnings	Exact identifier unii: 15FIX9V2JP
City Skin Age Defense Broad Spectrum SPF 50	TITANIUM DIOXIDE AND ZINC OXIDE	Murad, LLC	f8c572a2-b4bc-49e9-95df-359f05bd69b7	2025-03-28	Warnings	Exact identifier unii: 15FIX9V2JP
it cosmetics Your Skin But Better CC Plus Color Correcting Broad Spectrum SPF 50 Plus Sunscreen Full Coverage Deep FairLight Neutral Tan Rich Honey LightMedium and Neutral Medium	TITANIUM DIOXIDE AND ZINC OXIDE	IT COSMETICS, LLC	e17dc640-30e9-441b-a212-ef1508af7944	2025-03-25	Warnings	Exact identifier unii: 15FIX9V2JP
Vista Gonio Eye Lubricant	HYPROMELLOSE OPHTHALMIC SOLUTION	Red Wedding LLC	00da365d-2988-9c9e-e063-6294a90a8931	2025-03-25	Warnings	Exact identifier unii: B1QE5P712K
it cosmetics Your Skin But Better CC Plus Oil Free Matte Poreless Finish Full Coverage Broad Spectrum SPF 40 Sunscreen All Shades	TITANIUM DIOXIDE AND ZINC OXIDE	IT COSMETICS, LLC	b7d184fb-4a9a-4720-9b00-bf0caa257a8c	2025-03-25	Warnings	Exact identifier unii: 15FIX9V2JP
DOMINAS DARK SPOT TINTED SUNSCREEN	OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE	LG H&H CO., LTD.	2b6140cf-7e34-1658-e063-6394a90a3271	2025-03-24	Warnings	Exact identifier unii: 15FIX9V2JP
Etodolac	ETODOLAC	Preferred Pharmaceuticals Inc.	556a7d5f-2c3c-4efb-ac0c-fca140791602	2025-03-24	Boxed warning, Warnings, Adverse reactions	Exact identifier application number: ANDA076004 rxcui: 197686 unii: 2M36281008
NAKED SUNDAYS CABANA GLOW MINERAL GLOW SERUM DROPS Illuminating 40mL with Pink Algae SPF 50	TITANIUM OXIDE, ZINC OXIDE	NAKED SUNDAYS PTY LTD	01273e8c-aef0-d800-e063-6294a90abd49	2025-03-23	Warnings	Exact identifier unii: 15FIX9V2JP
NAKED SUNDAYS CABANA GLOW MINERAL GLOW SERUM DROPS BRONZE 40mL with wild Rosella SPF 50	TITANIUM OXIDE, ZINC OXIDE	NAKED SUNDAYS PTY LTD	01221d57-9eec-7e77-e063-6394a90a6042	2025-03-23	Warnings	Exact identifier unii: 15FIX9V2JP
NAKED SUNDAYS CABANA GLOW MINERAL GLOW SERUM DROPS Blush 40mL SPF 50	TITANIUM OXIDE, ZINC OXIDE	NAKED SUNDAYS PTY LTD	0ce809a1-45fb-9d4d-e063-6294a90a26a2	2025-03-23	Warnings	Exact identifier unii: 15FIX9V2JP
Impact Melanoma SPF 30	ZINC OXIDE	RENU LABORATORIES, LLC	f953302e-f712-129a-e053-6294a90ab9a8	2025-03-13	Warnings	Exact identifier unii: 15FIX9V2JP
Vertra Ehukai Beige Sunscreen Face Stick Broad Spectrum SPF 38	TITANIUM DIOXIDE	Eai-jr 286, Inc	303d5d5a-4c7a-1e23-e063-6294a90a0e58	2025-03-13	Warnings	Exact identifier unii: 15FIX9V2JP
RID Poison Ivy Rash Relief	CALAMINE AND ZINC OXIDE	Oystershell Consumer Health Inc.	36c3af9a-2646-4427-e063-6394a90a2c5e	2025-03-13	Warnings	Exact identifier unii: 1K09F3G675
Addiclenz	ASPARTAME, BENZALKONIUM CHLORIDE, FORMALINUM, METHYLENE CHLORIDE, METHYLPARABEN, PROPYLPARABEN, SODIUM BENZOATE, SODIUM CITRATE, TITANIUM DIOXIDE, ZINCUM OXYDATUM, ARSENICUM ALBUM, BETA VULGARIS, BISPHENOL A, BOLDO, CHELIDONIUM MAJUS, COBALTUM METALLICUM, CUPRUM METALLICUM, GLYPHOSATE, IODIUM, LYCOPODIUM CLAVATUM, PETROSELINUM SATIVUM, PHOSPHORICUM ACIDUM, SELENIUM METALLICUM, TARAXACUM OFFICINALE, ZINCUM METALLICUM	Deseret Biologicals, Inc.	25036c26-1c21-4e5a-b4db-b8e177458341	2025-03-11	Warnings	Exact identifier unii: 15FIX9V2JP

Reported adverse events (FAERS/openFDA)#

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