NDC 68071-1876-07 - Metronidazole

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
68071-1876
Requested NDC
68071-1876-07
Package NDCs from labels
68071-1876-1, 68071-1876-4, 68071-1876-2, 68071-1876-8, 68071-1876-3, 68071-1876-5, 68071-1876-0, 68071-1876-7, 68071-1876-07
Manufacturer
NuCare Pharmaceuticals, Inc.
Effective date
2026-08-26
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Metronidazole Tablets USPNuCare Pharmaceuticals, Inc.2026-08-26HUMAN PRESCRIPTION DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDCEffectiveRelated label
68071-1876-12024-07-16Metronidazole Tablets USP
68071-1876-12024-07-16Metronidazole Tablets USP
68071-1876-22024-07-16Metronidazole Tablets USP
68071-1876-22024-07-16Metronidazole Tablets USP
68071-1876-32024-07-16Metronidazole Tablets USP
68071-1876-32024-07-16Metronidazole Tablets USP
68071-1876-42024-07-16Metronidazole Tablets USP
68071-1876-42024-07-16Metronidazole Tablets USP
68071-1876-52024-07-16Metronidazole Tablets USP
68071-1876-52024-07-16Metronidazole Tablets USP
68071-1876-82024-07-16Metronidazole Tablets USP
68071-1876-82024-07-16Metronidazole Tablets USP
68071-1876-12023-01-30Metronidazole Tablets USP
68071-1876-12023-01-30Metronidazole Tablets USP
68071-1876-22023-01-30Metronidazole Tablets USP
68071-1876-22023-01-30Metronidazole Tablets USP
68071-1876-32023-01-30Metronidazole Tablets USP
68071-1876-32023-01-30Metronidazole Tablets USP
68071-1876-42023-01-30Metronidazole Tablets USP
68071-1876-42023-01-30Metronidazole Tablets USP
68071-1876-52023-01-30Metronidazole Tablets USP
68071-1876-52023-01-30Metronidazole Tablets USP
68071-1876-82023-01-30Metronidazole Tablets USP
68071-1876-82023-01-30Metronidazole Tablets USP
68071-1876-12021-02-12Metronidazole Tablets USP
68071-1876-12021-02-12Metronidazole Tablets USP
68071-1876-22021-02-12Metronidazole Tablets USP
68071-1876-22021-02-12Metronidazole Tablets USP
68071-1876-32021-02-12Metronidazole Tablets USP
68071-1876-32021-02-12Metronidazole Tablets USP
68071-1876-42021-02-12Metronidazole Tablets USP
68071-1876-42021-02-12Metronidazole Tablets USP
68071-1876-52021-02-12Metronidazole Tablets USP
68071-1876-52021-02-12Metronidazole Tablets USP
68071-1876-82021-02-12Metronidazole Tablets USP
68071-1876-82021-02-12Metronidazole Tablets USP
68071-1876-12021-01-29Metronidazole Tablets USP
68071-1876-12021-01-29Metronidazole Tablets USP
68071-1876-22021-01-29Metronidazole Tablets USP
68071-1876-22021-01-29Metronidazole Tablets USP
68071-1876-32021-01-29Metronidazole Tablets USP
68071-1876-32021-01-29Metronidazole Tablets USP
68071-1876-42021-01-29Metronidazole Tablets USP
68071-1876-42021-01-29Metronidazole Tablets USP
68071-1876-52021-01-29Metronidazole Tablets USP
68071-1876-52021-01-29Metronidazole Tablets USP
68071-1876-82021-01-29Metronidazole Tablets USP
68071-1876-82021-01-29Metronidazole Tablets USP

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68071-1876-0Metronidazole42 in 1 BOTTLETABLET, FILM COATED428
68071-1876-1Metronidazole4 in 1 BOTTLETABLET, FILM COATED48
68071-1876-2Metronidazole21 in 1 BOTTLETABLET, FILM COATED218
68071-1876-3Metronidazole30 in 1 BOTTLETABLET, FILM COATED308
68071-1876-4Metronidazole14 in 1 BOTTLETABLET, FILM COATED148
68071-1876-5Metronidazole40 in 1 BOTTLETABLET, FILM COATED408
68071-1876-8Metronidazole28 in 1 BOTTLETABLET, FILM COATED288

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68071-1876METRONIDAZOLE TABLET, FILM COATED [NUCARE PHARMACEUTICALS, INC.]7Current NDC, Legacy NDC, 7 package rows20250104_4040db14-750f-6d20-e054-00144ff8d46c.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 9 of 115 · 2,289 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Blue Lizard Sport SPF 50 SunscreenOCTISALATE AND TITANIUM DIOXIDE AND ZINC OXIDECrown Laboratories4955fa1c-789d-4f42-af75-70223310644a2026-05-01WarningsExact identifier
unii: 15FIX9V2JP
Blue Lizard Kids SPF 50 SunscreenOCTISALATE AND TITANIUM DIOXIDE AND ZINC OXIDECrown Laboratoriesba4ae906-48c0-8384-e053-2995a90afb912026-05-01WarningsExact identifier
unii: 15FIX9V2JP
metronidazoleMETRONIDAZOLEST. MARY'S MEDICAL PARK PHARMACYe3a32908-9db1-6ca7-e053-2a95a90a82fb2026-05-01Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 311681
unii: 140QMO216E
Dior Backstage Glow-Up Skin Tint Tinted Moisturizer SPF 20 2CR Cool RosyOCTISALATE, TITANIUM DIOXIDEParfums Christian Dior6831832a-e52e-43ea-899f-f5d44bea5a942026-04-30WarningsExact identifier
unii: 15FIX9V2JP
Tru Skin Rituals SPF 25TITANIUM DIOXIDE, ZINC OXIDESpa de Soleilf725cd5c-999e-2393-e053-6394a90a09dc2026-04-30WarningsExact identifier
unii: 15FIX9V2JP
MetronidazoleMETRONIDAZOLECoupler LLC509c8d03-e199-8154-e063-6394a90afddc2026-04-29Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA203458
rxcui: 311681
unii: 140QMO216E
TiZO2TITANIUM DIOXIDE, ZINC OXIDEFallien Cosmeceuticals Ltd.509cad98-0321-2a0a-e063-6294a90a6ea92026-04-29WarningsExact identifier
unii: 15FIX9V2JP
TiZO2TITANIUM DIOXIDE, ZINC OXIDEFallien Cosmeceuticals Ltd.509d7206-0cc1-c997-e063-6294a90a89e02026-04-29WarningsExact identifier
unii: 15FIX9V2JP
JMSOLUTION SKIN BOOST NIACINAMIDE SUNSCREENHOMOSALATE, OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDEGPNY CORP211dea04-faad-8ffc-e063-6294a90a8d682026-04-29WarningsExact identifier
unii: 15FIX9V2JP
GoodSense Eye Drops Advanced Relief MoisturizerDEXTRAN, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HCLPreferred PHarmaceuticals Inc.011473a8-26d5-4661-b3c0-745f9b6aa1d82026-04-29WarningsExact identifier
unii: B697894SGQ
Anything SPFOCTINOXATE, OCTISALATE, ZINC OXIDE, AVOBENZONE, HOMOSALATE, TITANIUM DIOXIDEAnything SPF LLC508b8dcb-6600-6dad-e063-6294a90a565a2026-04-28WarningsExact identifier
unii: 15FIX9V2JP
METRONIDAZOLEMETRONIDAZOLEB. Braun Medical Inc.fd191c06-9d3b-4e46-9f79-90f6af6149472026-04-23Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 140QMO216E
Johnsons Baby Mineral Sunscreen SPF 30TITANIUM DIOXIDE, ZINC OXIDEKenvue Brands LLC4fe04c4b-2751-0561-e063-6394a90af7682026-04-22WarningsExact identifier
unii: 15FIX9V2JP
Lazy Face SPF 30 FacescreenTITANIUM DIOXIDE, ZINC OXIDESunny Day Creations500ee303-7302-68d5-e063-6394a90ac6d42026-04-22WarningsExact identifier
unii: 15FIX9V2JP
ELROEL Pang Pang Sun Cushion S7ZINC OXIDE, TITANIUM DIOXIDE, OCTINOXATE, OCTISALATEMONOGLOT HOLDINGS Inc.256bf56f-aefa-47ce-890c-5a3896c11b922026-04-17WarningsExact identifier
unii: 15FIX9V2JP
JUNGSAEMMOOL Essential Skin Nuder Cushion FairTITANIUM DIOXIDE, OCTINOXATE, OCTISALATEJungsaemmool Beauty Co., Ltd.3a43c7c0-7468-4b7a-95b9-f03e37f1b49b2026-04-17WarningsExact identifier
unii: 15FIX9V2JP
JUNGSAEMMOOL Essential Skin Nuder Cushion Fair LightTITANIUM DIOXIDE, OCTINOXATE, OCTISALATEJungsaemmool Beauty Co., Ltd.a251eb20-02e6-4b55-b969-c1bef2f9d7322026-04-17WarningsExact identifier
unii: 15FIX9V2JP
JUNGSAEMMOOL Essential Skin Nuder Cushion Fair PinkTITANIUM DIOXIDE, OCTINOXATE, OCTISALATEJungsaemmool Beauty Co., Ltd.6684d69a-89ff-41e8-81f0-3e2367811a182026-04-17WarningsExact identifier
unii: 15FIX9V2JP
JUNGSAEMMOOL Essential Skin Nuder Cushion LightTITANIUM DIOXIDE, OCTINOXATE, OCTISALATEJungsaemmool Beauty Co., Ltd.bf24d081-85f7-4a26-9416-ecff1fe59dec2026-04-17WarningsExact identifier
unii: 15FIX9V2JP
JUNGSAEMMOOL Essential Skin Nuder Cushion Pink LightTITANIUM DIOXIDE, OCTINOXATE, OCTISALATEJungsaemmool Beauty Co., Ltd.4a09a01a-404f-4b67-91e0-666153f550e82026-04-17WarningsExact identifier
unii: 15FIX9V2JP

Reported adverse events (FAERS/openFDA)#

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