NDC 0002-3270-01 - Cymbalta

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: 0002-3270
Requested NDC: 0002-3270-01
Package NDCs from labels: 0002-3270-30, 0002-3270-01
Manufacturer: Eli Lilly and Company
Effective date: 2025-07-21
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Cymbalta - Eli Lilly and Company	Eli Lilly and Company	2025-07-21	HUMAN PRESCRIPTION DRUG LABEL
Cymbalta - PD-Rx Pharmaceuticals, Inc.	PD-Rx Pharmaceuticals, Inc.	2022-02-17	HUMAN PRESCRIPTION DRUG LABEL
Cymbalta	H.J. Harkins Company, Inc. \| Eli Lilly and Company \| Evonik Degussa Corporation \| Lilly del Caribe, Inc. (PR06) \| Lilly del Caribe, Inc. (PR01) \| Eli Lilly and Company (Indianapolis) \| Sharp - Conshohocken \| Sharp - Allentown	2011-10-18	HUMAN PRESCRIPTION DRUG LABEL
National Council for Prescription Drug Programs indexing - billing unit	National Council for Prescription Drug Programs	2012-07-24	Indexing - Billing Unit

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
0002-3270-30	Cymbalta	30 in 1 BOTTLE	CAPSULE, DELAYED RELEASE	30		90

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0002-3270	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [ELI LILLY AND COMPANY]	89	Legacy NDC, 1 package rows	20241206_2f7d4d67-10c1-4bf4-a7f2-c185fbad64ba.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0002-3270-01	EA - Each	0002-3270	7149c6ef-ec54-4fd3-9083-2e15125bea62	1	2012-07-24
0002-3270-04	EA - Each	0002-3270	ad73f24c-7d72-4830-97ae-1a9ba1b8ec58	1	2012-07-24
0002-3270-30	EA - Each	0002-3270	581237c9-1b60-4246-8dff-bfaab7eb8898	1	2012-07-24
0002-3270-33	EA - Each	0002-3270	9366b8c5-1181-45d4-8587-e383e34e2a45	1	2012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
Duloxetine hydrochloride	ACTIVE INGREDIENT	9044SC542W	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [ELI LILLY AND COMPANY]	66
Duloxetine	ACTIVE MOIETY	O5TNM5N07U	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [ELI LILLY AND COMPANY]	66
FD&C BLUE NO. 2	INACTIVE INGREDIENT	L06K8R7DQK	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [ELI LILLY AND COMPANY]	66
FERRIC OXIDE YELLOW	INACTIVE INGREDIENT	EX438O2MRT	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [ELI LILLY AND COMPANY]	66
Gelatin	INACTIVE INGREDIENT	2G86QN327L	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [ELI LILLY AND COMPANY]	66
HYPROMELLOSE ACETATE SUCCINATE 16070722 (3 MM2/S)	INACTIVE INGREDIENT	24P2YXD2PW	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [ELI LILLY AND COMPANY]	66
Hypromelloses	INACTIVE INGREDIENT	3NXW29V3WO	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [ELI LILLY AND COMPANY]	66
Sodium lauryl sulfate	INACTIVE INGREDIENT	368GB5141J	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [ELI LILLY AND COMPANY]	66
Sucrose	INACTIVE INGREDIENT	C151H8M554	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [ELI LILLY AND COMPANY]	66
Talc	INACTIVE INGREDIENT	7SEV7J4R1U	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [ELI LILLY AND COMPANY]	66
Titanium dioxide	INACTIVE INGREDIENT	15FIX9V2JP	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [ELI LILLY AND COMPANY]	66
Triethyl citrate	INACTIVE INGREDIENT	8Z96QXD6UM	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [ELI LILLY AND COMPANY]	66
Duloxetine hydrochloride	ACTIVE INGREDIENT	9044SC542W	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [PD-RX PHARMACEUTICALS, INC.]	45
Duloxetine	ACTIVE MOIETY	O5TNM5N07U	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [PD-RX PHARMACEUTICALS, INC.]	45
FD&C BLUE NO. 2	INACTIVE INGREDIENT	L06K8R7DQK	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [PD-RX PHARMACEUTICALS, INC.]	45
FERRIC OXIDE YELLOW	INACTIVE INGREDIENT	EX438O2MRT	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [PD-RX PHARMACEUTICALS, INC.]	45
Gelatin	INACTIVE INGREDIENT	2G86QN327L	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [PD-RX PHARMACEUTICALS, INC.]	45
HYPROMELLOSE ACETATE SUCCINATE 16070722 (3 MM2/S)	INACTIVE INGREDIENT	24P2YXD2PW	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [PD-RX PHARMACEUTICALS, INC.]	45
Hypromelloses	INACTIVE INGREDIENT	3NXW29V3WO	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [PD-RX PHARMACEUTICALS, INC.]	45
Sodium lauryl sulfate	INACTIVE INGREDIENT	368GB5141J	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [PD-RX PHARMACEUTICALS, INC.]	45
Sucrose	INACTIVE INGREDIENT	C151H8M554	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [PD-RX PHARMACEUTICALS, INC.]	45
Talc	INACTIVE INGREDIENT	7SEV7J4R1U	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [PD-RX PHARMACEUTICALS, INC.]	45
Titanium dioxide	INACTIVE INGREDIENT	15FIX9V2JP	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [PD-RX PHARMACEUTICALS, INC.]	45
Triethyl citrate	INACTIVE INGREDIENT	8Z96QXD6UM	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [PD-RX PHARMACEUTICALS, INC.]	45
Duloxetine hydrochloride	ACTIVE INGREDIENT	9044SC542W	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [H.J. HARKINS COMPANY, INC.]	1
Duloxetine	ACTIVE MOIETY	O5TNM5N07U	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [H.J. HARKINS COMPANY, INC.]	1
FD&C BLUE NO. 2	INACTIVE INGREDIENT	L06K8R7DQK	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [H.J. HARKINS COMPANY, INC.]	1
FERRIC OXIDE YELLOW	INACTIVE INGREDIENT	EX438O2MRT	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [H.J. HARKINS COMPANY, INC.]	1
Gelatin	INACTIVE INGREDIENT	2G86QN327L	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [H.J. HARKINS COMPANY, INC.]	1
HYPROMELLOSE ACETATE SUCCINATE 16070722 (3 MM2/S)	INACTIVE INGREDIENT	24P2YXD2PW	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [H.J. HARKINS COMPANY, INC.]	1
Hypromelloses	INACTIVE INGREDIENT	3NXW29V3WO	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [H.J. HARKINS COMPANY, INC.]	1
Sodium lauryl sulfate	INACTIVE INGREDIENT	368GB5141J	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [H.J. HARKINS COMPANY, INC.]	1
Sucrose	INACTIVE INGREDIENT	C151H8M554	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [H.J. HARKINS COMPANY, INC.]	1
Talc	INACTIVE INGREDIENT	7SEV7J4R1U	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [H.J. HARKINS COMPANY, INC.]	1
Titanium dioxide	INACTIVE INGREDIENT	15FIX9V2JP	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [H.J. HARKINS COMPANY, INC.]	1
Triethyl citrate	INACTIVE INGREDIENT	8Z96QXD6UM	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [H.J. HARKINS COMPANY, INC.]	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 12 of 112 · 2,231 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Nu Colour Bioadaptive BB plus Foundation - Beige	TITANIUM DIOXIDE	NSE Products, Inc.	f74e83fe-41a0-4998-ae53-30ed5af47592	2026-04-07	Warnings	Exact identifier unii: 15FIX9V2JP
LensMate Preservative-Free Artificial Tears	LUBRICANT EYE DROPS	YD BIO USA, INC.	4ebacb2b-9b2d-6bc1-e063-6294a90a3426	2026-04-05	Warnings	Exact identifier unii: 3NXW29V3WO
Exovisse Preservative-Free Artificial Tears	LUBRICANT EYE GEL DROPS	YD BIO USA, INC.	4ebc154b-128b-9dde-e063-6294a90ae00e	2026-04-05	Warnings	Exact identifier unii: 3NXW29V3WO
EltaMD Skincare UV AOX Elements SPF50 Tinted	TITANIUM DIOXIDE, ZINC OXIDE SUNSCREEN	CP Skin Health Group, Inc	2c74209d-9b88-4c32-ad42-cd6de16c1fef	2026-04-03	Warnings	Exact identifier unii: 15FIX9V2JP
EltaMD UV Restore Tinted	TITANIUM DIOXIDE AND ZINC OXIDE SUNSCREEN	CP Skin Health Group, Inc	4fc18856-01b3-43ed-9e1b-b4394e31aa3c	2026-04-03	Warnings	Exact identifier unii: 15FIX9V2JP
Sunscreen for baby SPF50plus	OCTOCRYLENE,ETHYLHEXYL METHOXYCINNAMATE,TITANIUM DIOXIDE,ETHYLHEXYL SALICYLATE	Guangzhou Senmai Biotechnology Co., Ltd.	1cb7fbca-0874-ae53-e063-6294a90ab42a	2026-04-02	Warnings	Exact identifier unii: 15FIX9V2JP
TiZO3	TITANIUM DIOXIDE, ZINC OXIDE	Fallien Cosmeceuticals, LTD	4e7bdec2-abcc-0267-e063-6394a90ae47a	2026-04-02	Warnings	Exact identifier unii: 15FIX9V2JP
EltaMD UV Restore	TITANIUM DIOXIDE, ZINC OXIDE SUNSCREEN	CP Skin Health Group, Inc	17b47994-82d6-4f9d-8249-bdb55106c9b3	2026-04-02	Warnings	Exact identifier unii: 15FIX9V2JP
Clinical Skin Filter Tinted Sunscreen	CLINICAL SKIN FILTER TINTED SUNSCREEN	BY KIN AESTHETICS LLC	4e69a8a3-8dbb-577a-e063-6294a90a6a23	2026-04-01	Warnings	Exact identifier unii: 15FIX9V2JP
Krx Aesthetics All Day Glow Sunblocker	KRX AESTHETICS ALL DAY GLOW SUNBLOCKER	BY KIN AESTHETICS LLC	4e69df43-393b-bc09-e063-6394a90a275a	2026-04-01	Warnings	Exact identifier unii: 15FIX9V2JP
spf 50 mineral powder sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	Smalls Brand LLC DBA Roe Wellness	f8762dd1-0484-74ea-e053-6294a90ac112	2026-03-31	Warnings	Exact identifier unii: 15FIX9V2JP
SeranovaTM ULTRALIGHT SPF50 SERUM	SERANOVATM ULTRALIGHT SPF50 SERUM	Guangzhou Ariel Biotech Co., Ltd.	4e5d716d-2b2d-d42f-e063-6294a90a1e52	2026-03-31	Warnings	Exact identifier unii: 15FIX9V2JP
Duloxetine	DULOXETINE	NuCare Pharmaceuticals, Inc.	4e42a04a-ab8e-3ec9-e063-6394a90a4565	2026-03-30	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 596926 unii: 9044SC542W
UV SOLUTIONS BRIGHTENING TINTED BROAD SPECTRUM SPF 50 SUNSCREEN NIACINAMIDE ANTIOXIDANTS DARK SHADE	TITANIUM DIOXIDE AND ZINC OXIDE	CLINIQUE LABORATORIES LLC	4e0bd355-99c6-8cf4-e063-6294a90ab4b3	2026-03-27	Warnings	Exact identifier unii: 15FIX9V2JP
Crocodile Tears Lubricant Eye Drops	GLYCERIN, HYPROMELLOSE, POLYETHYLENE GLYCOL 400	Crocodile Tears LLC	4df29336-ea0c-0484-e063-6294a90a685a	2026-03-26	Warnings	Exact identifier unii: 3NXW29V3WO
SUNNYSIDEKICK UVA/UVB Broad Spectrum SPF 30 Brush-On Mineral	ZINC OXIDE, TITANIUM DIOXIDE	Classic Cosmetics LLC	4df3b8c0-71bc-acdd-e063-6394a90a35c0	2026-03-26	Warnings	Exact identifier unii: 15FIX9V2JP
Silkscreen Sheer Tint Mineral Light-Medium	TITANIUM DIOXIDE, ZINC OXIDE	Curology	4ddbe349-6880-a5fc-e063-6294a90a275c	2026-03-25	Warnings	Exact identifier unii: 15FIX9V2JP
Artificial Tears Lubricant Eye Drops	GLYCERIN, HYPROMELLOSE, POLYETHYLENE GLYCOL 400	KC Pharmaceuticals, Inc	4de5c844-85ca-ff9f-e063-6394a90ac12c	2026-03-25	Warnings	Exact identifier unii: 3NXW29V3WO
BANANA BOAT	TITANIUM DIOXIDE,ZINC OXIDE	Edgewell Personal Care Brands LLC	4e0450ca-147a-91d7-e063-6394a90ae73b	2026-03-25	Warnings	Exact identifier unii: 15FIX9V2JP
Sunscreen SPF 50	SUNSCREEN SPF 50	Guangzhou Ariel Biotech Co., Ltd.	4dd05620-30a3-9cea-e063-6294a90af18b	2026-03-24	Warnings	Exact identifier unii: 15FIX9V2JP

Reported adverse events (FAERS/openFDA)#

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