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 3 of 115 · 2,289 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
MetronidazoleMETRONIDAZOLESun Pharmaceutical Industries, Inc.5842a554-58d1-4ee4-99aa-1e6029a69be22026-07-15Warnings, Adverse reactionsExact identifier
unii: 140QMO216E
MetronidazoleMETRONIDAZOLEBryant Ranch Prepack4748ba37-9d66-497d-aa9f-ca2d541c5f412026-07-15Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 311681
unii: 140QMO216E
MetronidazoleMETRONIDAZOLEPreferred Pharmaceuticals Inc.59e53582-244a-4e9d-b18e-75dddc6a50522026-07-08Adverse reactionsExact identifier
unii: 140QMO216E
Bombee Honey Daily Glow Shield SunscreenHOMOSALATE, OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDEABT ASIA Inc.56112dff-b091-7a56-e063-6294a90a77d32026-07-08WarningsExact identifier
unii: 15FIX9V2JP
Stay Ageless Tinted Mineral SunscreenBROAD SPECTRUM SPF30DERMIO DERMATOLOGY LLC562f5b0d-6a10-305d-e063-6394a90a59802026-07-08WarningsExact identifier
unii: 15FIX9V2JP
Stay Ageless Tinted Mineral SunscreenBROAD SPECTRUM SPF30Suzanne's Skin2soul LLC562fbaa6-f93a-5ec4-e063-6294a90a96342026-07-08WarningsExact identifier
unii: 15FIX9V2JP
Aussie Betta Tallow Sunscreen SPF50 SPF50TITANIUM DIOXIDE AND ZINC OXIDE SUNSCREENAUSSIE BETTA HEALTHY CARE PTY LTD56007d82-ff5b-6c26-e063-6294a90a09b62026-07-07WarningsExact identifier
unii: 15FIX9V2JP
MetronidazoleMETRONIDAZOLEREMEDYREPACK INC.cfeab9e3-58b9-4890-9185-11b62904e2af2026-07-07Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA203458
rxcui: 314106
unii: 140QMO216E
EELHOE Body Coverage PerfectorTITANIUM DIOXIDEShantou Eelhoe Daily Chemical Technology Co., Ltd.5610c3b7-456b-3bc1-e063-6394a90a3fa82026-07-07WarningsExact identifier
unii: 15FIX9V2JP
MetronidazoleMETRONIDAZOLEPreferred Pharmaceuticals Inc.cbee69e8-029c-49d2-89cd-f504b8e0ac282026-07-07Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA203458
rxcui: 311681
unii: 140QMO216E
MetronidazoleMETRONIDAZOLEPreferred Pharmaceuticals Inc.3e0a14f1-961b-4722-bfea-aafcc5d7706c2026-07-07Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA203458
rxcui: 314106
unii: 140QMO216E
Premier Tinted Mineral SunscreenBROAD SPECTRUM SPF30Emerald Aesthetics LLC55f88dd1-346c-22a5-e063-6294a90a711f2026-07-06WarningsExact identifier
unii: 15FIX9V2JP
MetronidazoleMETRONIDAZOLEREMEDYREPACK INC.53918705-d2fe-4c6b-9501-a619a8ad39912026-07-03Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 311681
unii: 140QMO216E
OHUI Ultimate Cover CC Cushion Compact 02 Natural BeigeTITANIUM DIOXIDELG H&H Co., Ltd.d307471c-6cc6-ce48-e053-2995a90a3e022026-07-02WarningsExact identifier
unii: 15FIX9V2JP
Evereden Fluid Silk Mineral Sunscreen PRO SPF50TITANIUM DIOXIDE, ZINC OXIDEEden Brands Inc.2cb7773f-9a05-ad02-e063-6294a90af0242026-07-01WarningsExact identifier
unii: 15FIX9V2JP
MetronidazoleMETRONIDAZOLEKanchan Healthcare Inc8836334e-6db4-44be-bc9e-099b26322cf42026-07-01Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 314106
rxcui: 311681
unii: 140QMO216E
OHUI Ultimate Cover CC Cushion Compact 01 Light BeigeTITANIUM DIOXIDELG H&H Co., Ltd.d2f9c54b-ac4e-5141-e053-2a95a90aa2b82026-06-30WarningsExact identifier
unii: 15FIX9V2JP
metronidazoleMETRONIDAZOLEBryant Ranch Prepack99886f54-4ebe-4a2d-b779-bcfbb0634db12026-06-30Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 140QMO216E
TOCOBO Blur Finish Sun Cushion Cotton BlueHOMOSALATE, OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDEPICTON Co., Ltd.4d6ddee3-9a76-6c9c-e063-6394a90a15292026-06-29WarningsExact identifier
unii: 15FIX9V2JP
PYLERABISMUTH SUBCITRATE POTASSIUM, METRONIDAZOLE, AND TETRACYCLINE HYDROCHLORIDEH2-Pharma, LLC5cdacbf5-67be-42eb-bd54-8acc32ea1abc2026-06-29Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 140QMO216E

Reported adverse events (FAERS/openFDA)#

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