NDC 58602-705-03 - Famotidine

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
58602-705
Requested NDC
58602-705-03
Package NDCs from labels
58602-705-15, 58602-705-19, 58602-705-84, 58602-705-03, 58602-705-09, 58602-705-12, 58602-705-93, 58602-705-14, 58602-705-34, 58602-705-39, 58602-705-44, 58602-705-40, 58602-705-88, 58602-705-41, 58602-705-32
Manufacturer
Aurohealth LLC | Aurobindo Pharma Limited | APL HEALTHCARE LIMITED
Effective date
2025-03-15
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Famotidine - Aurohealth LLC | Aurobindo Pharma Limited | APL HEALTHCARE LIMITEDAurohealth LLC | Aurobindo Pharma Limited | APL HEALTHCARE LIMITED2025-03-15Human OTC Drug Label
Famotidine - Proficient Rx LPProficient Rx LP2022-06-01HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58602-705-03Famotidine10 in 1 BLISTER PACKTABLET, FILM COATED1013
58602-705-09Famotidine3 in 1 CARTONTABLET, FILM COATED313
58602-705-12Famotidine4 in 1 CARTONTABLET, FILM COATED413
58602-705-14Famotidine1 in 1 CARTONTABLET, FILM COATED113
58602-705-14Famotidine50 in 1 BOTTLETABLET, FILM COATED5013
58602-705-15Famotidine1 in 1 CARTONTABLET, FILM COATED113
58602-705-15Famotidine60 in 1 BOTTLETABLET, FILM COATED6013
58602-705-19Famotidine1 in 1 CARTONTABLET, FILM COATED113
58602-705-19Famotidine90 in 1 BOTTLETABLET, FILM COATED9013
58602-705-32Famotidine180 in 1 BOTTLETABLET, FILM COATED18013
58602-705-32Famotidine1 in 1 CARTONTABLET, FILM COATED113
58602-705-34Famotidine1 in 1 CARTONTABLET, FILM COATED113
58602-705-34Famotidine200 in 1 BOTTLETABLET, FILM COATED20013
58602-705-39Famotidine1 in 1 CARTONTABLET, FILM COATED113
58602-705-39Famotidine365 in 1 BOTTLETABLET, FILM COATED36513
58602-705-40Famotidine500 in 1 BOTTLETABLET, FILM COATED50013
58602-705-40Famotidine1 in 1 CARTONTABLET, FILM COATED113
58602-705-41Famotidine1000 in 1 BOTTLETABLET, FILM COATED100013
58602-705-41Famotidine1 in 1 CARTONTABLET, FILM COATED113
58602-705-44Famotidine1 in 1 CARTONTABLET, FILM COATED113
58602-705-44Famotidine400 in 1 BOTTLETABLET, FILM COATED40013
58602-705-84Famotidine1 in 1 CARTONTABLET, FILM COATED113
58602-705-84Famotidine30 in 1 BOTTLETABLET, FILM COATED3013
58602-705-88Famotidine750 in 1 BOTTLETABLET, FILM COATED75013
58602-705-88Famotidine1 in 1 CARTONTABLET, FILM COATED113
58602-705-93Famotidine90 in 1 BOTTLETABLET, FILM COATED9013

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58602-705FAMOTIDINE TABLET, FILM COATED [AUROHEALTH LLC]13Current NDC, Legacy NDC, 26 package rows20250321_756c7234-6a63-4b1b-be36-2b1ed09e67a0.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
58602-705-15EA - Each58602-705f2623aa0-791a-40af-ac34-8254bc52f7c912022-02-07
58602-705-19EA - Each58602-7056402435b-39ad-40bf-aadd-6feba559e09812021-04-08
58602-705-84EA - Each58602-70571d62bb7-0854-4a7b-9efa-f26c2d6522d612020-07-13

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 7 of 122 · 2,434 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ANESSA PERFECT UV SUNSCREEN SKINCARE MILK GBZINC OXIDE OCTOCRYLENE ETHYLHEXYL SALICYLATE HOMOSALATE TITANIUM DIOXIDEHONGKONG JIAHE INTERNATIONAL HOLDING LIMITED5354af18-50c4-5fba-e063-6394a90ace392026-06-03WarningsExact identifier
unii: 15FIX9V2JP
ACID REDUCERFAMOTIDINEHyVee Inc381db08e-5756-4255-8202-1d8e6a1cf0382026-06-03WarningsExact identifier
unii: 5QZO15J2Z8
ATOMY BB SUNSCREENTITANIUM DIOXIDE, ZINC OXIDEATOMY CO., LTD.b0cd27ee-4917-4800-bcdf-c6e14b28c1d12026-06-02WarningsExact identifier
unii: 15FIX9V2JP
Atomy Sunscreen White Broad Spectrum SPF 50 PLUSHOMOSALATE, OCTISALATE, TITANIUM DIOXIDE, ZINC OXIDEATOMY CO., LTD.ad0b9091-a990-45bf-93f4-d886be1bbffe2026-06-02WarningsExact identifier
unii: 15FIX9V2JP
Atomy Sunscreen Beige Broad Spectrum SPF 50 PLUSHOMOSALATE, OCTISALATE, TITANIUM DIOXIDE, ZINC OXIDEATOMY CO., LTD.994d5680-284e-4faf-a29b-4d28f8d46e8f2026-06-02WarningsExact identifier
unii: 15FIX9V2JP
FamotidineFAMOTIDINESt. Mary's Medical Park Pharmacyf175822d-7ca4-fa33-e053-2995a90ac3102026-06-02Warnings, Adverse reactionsExact identifier
unii: 5QZO15J2Z8
Matte Veil Tinted Broad Spectrum Sunscreen SPF 40ZINC OXIDE, TITANIUM DIOXIDEPrivate Label Skin Carea8d60212-18a7-42af-8bb3-bfcff7690a492026-06-02WarningsExact identifier
unii: 15FIX9V2JP
The Mineral Melt SPF30ZINC OXIDE, TITANIUM DIOXIDEDune Suncare Inc.2114fc3b-c8ce-45d2-8a82-4dc54f0adaf32026-06-02WarningsExact identifier
unii: 15FIX9V2JP
Good Neighbor Pharmacy Dual Action CompleteFAMOTIDINE, CALCIUM CARBONATE AND MAGNESIUM HYDROXIDEAmerisource Bergenb7453c0e-b452-409b-a324-83fdd105bfd02026-06-02WarningsExact identifier
unii: 5QZO15J2Z8
LA ROCHE POSAY LABORATOIRE DERMATOLOGIQUE ANTHELIOS UV AIR MINERAL SERUM SUNSCREEN BROAD SPECTRUM SPF 50TITANIUM DIOXIDE AND ZINC OXIDELOreal USA Products Inca1acb789-5bf4-4447-b3c5-4a7d4d3013a72026-06-01WarningsExact identifier
unii: 15FIX9V2JP
Pepcid CompleteFAMOTIDINE, CALCIUM CARBONATE, AND MAGNESIUM HYDROXIDESavings Distributors LLC549136d5-8f2c-d417-e063-6394a90a23e42026-06-01WarningsExact identifier
unii: 5QZO15J2Z8
FamotidineFAMOTIDINEProficient Rx LP68d21d95-9603-4e68-855a-bfc65b1b58c32026-06-01Warnings, Adverse reactionsExact identifier
unii: 5QZO15J2Z8
Dual Action CompleteFAMOTIDINE, CALCIUM CARBONATE, MAGNESIUM HYDROXIDEMeijer Distribution Inc50fe57e1-6678-4697-9b35-4673db67d4fb2026-06-01WarningsExact identifier
unii: 5QZO15J2Z8
KIEHLS DERMATOLOGIST SOLUTIONS BETTER SCREEN MINER ALL UV SERUM BROAD SPECTRUM SPF 50 PLUS MINERAL SUNSCREENTITANIUM DIOXIDE AND ZINC OXIDELOreal USA Products Inc294e6049-12b5-4b45-ae00-8ee1d9d2a1a42026-05-29WarningsExact identifier
unii: 15FIX9V2JP
FAMOTIDINEFAMOTIDINEA-S Medication Solutionse53928f3-5181-490b-acfb-be8d4cea60a92026-05-29Warnings, Adverse reactionsExact identifier
unii: 5QZO15J2Z8
FAMOTIDINEFAMOTIDINEA-S Medication Solutions05b47b1d-f7f3-4dae-9b22-d43d2a7cfaef2026-05-29Warnings, Adverse reactionsExact identifier
unii: 5QZO15J2Z8
CalamineCALAMINE AND ZINC OXIDEPharma Nobis, LLCfbcfa541-beda-06de-e053-6294a90a92982026-05-26WarningsExact identifier
unii: 1K09F3G675
O HUI DAY SHIELD PERFECT SUN BLACK BROAD SPECTRUM SPF 50 SUNSCREENOCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDELG H&H Co., Ltd.52ba9423-8b9b-38f7-e063-6394a90a95da2026-05-26WarningsExact identifier
unii: 15FIX9V2JP
Mineral SPF 30 MoisturizerMINERAL SPF 30 MOISTURIZERDont Run Out Inc (DBA: Public Goods)52462e7e-0c2c-6b64-e063-6394a90a42302026-05-21WarningsExact identifier
unii: 15FIX9V2JP
DRMTLGY Radiance PowderTITANIUM DIOXIDE, ZINC OXIDEDRMTLGY15bda8d5-8c3c-6ba5-e063-6394a90a82d92026-05-21WarningsExact identifier
unii: 15FIX9V2JP

Reported adverse events (FAERS/openFDA)#

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