FDA.reportPublic FDA data

NDC 70710-1775-05 - atorvastatin calcium

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
70710-1775
Requested NDC
70710-1775-05
Package NDCs from labels
70710-1775-9, 70710-1775-5, 70710-1775-0, 70710-1775-05
Manufacturer
A-S Medication Solutions
Effective date
2025-10-21
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
atorvastatin calcium - A-S Medication SolutionsA-S Medication Solutions2025-10-21HUMAN PRESCRIPTION DRUG LABEL
atorvastatin calcium - A-S Medication SolutionsA-S Medication Solutions2025-10-21HUMAN PRESCRIPTION DRUG LABEL
atorvastatin calcium - Zydus Pharmaceuticals USA Inc. | Zydus Lifesciences Limited | Zydus Pharmaceuticals LimitedZydus Pharmaceuticals USA Inc. | Zydus Lifesciences Limited | Zydus Pharmaceuticals Limited2025-05-30HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70710-1775-0atorvastatin calcium1000 in 1 BOTTLETABLET10003
70710-1775-5atorvastatin calcium500 in 1 BOTTLETABLET5003
70710-1775-9atorvastatin calcium90 in 1 BOTTLETABLET903

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70710-1775ATORVASTATIN CALCIUM TABLET [ZYDUS PHARMACEUTICALS USA INC.]2Current NDC, 3 package rows20240618_55ad4a90-d177-4cce-b7ec-cb75067f6c14.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
70710-1775-0EA - Each70710-1775a646afd8-ac06-42ed-8811-b90381c8edfb12024-08-12
70710-1775-9EA - Each70710-1775e45202fb-a6b5-4ef4-b5d8-2e053d62c66812024-08-12

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 118 of 147 · 2,921 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Regular Strength AntacidCALCIUM CARBONATEAmerisource Bergenf9dd2797-c804-43c4-9d64-47de3b63a19a2024-06-28WarningsExact identifier
unii: H0G9379FGK
LOreal Paris Visible Lift Serum Absolute Advanced Makeup Broad Spectrum SPF 17 SunscreenOCTINOXATE AND TITANIUM DIOXIDEL'Oreal USA Products Inc8598d56b-adcd-48e8-b6fc-77bc934009c72024-06-27WarningsExact identifier
unii: 15FIX9V2JP
Lancome Paris Teint Idole Ultra Wear Breathable Coverage Foundation Reno Broad Spectrum SPF 25 SunscreenOCTINOXATE AND TITANIUM DIOXIDEL'Oreal USA Products Incbe2a83fb-e4f8-4313-b5bd-150f351fb3452024-06-26WarningsExact identifier
unii: 15FIX9V2JP
Lancome Paris Teint Idole Ultra Wear Breathable Coverage Foundation Reno Broad Spectrum SPF 25 SunscreenOCTINOXATE AND TITANIUM DIOXIDESICOS ET CIE066a0951-2e7e-40c0-8035-4d708a32f16c2024-06-26WarningsExact identifier
unii: 15FIX9V2JP
Ultra Strength Antacid Assorted FruitCALCIUM CARBONATEAmerisource Bergend39b3a19-b0e7-409d-9e0b-ef847fe8be2f2024-06-26WarningsExact identifier
unii: H0G9379FGK
Yves Saint Laurent All Hours Foundation Broad Spectrum SPF 30 Sunscreen Luminous Matte FoundationOCTINOXATE AND TITANIUM DIOXIDESICOS ET CIE66a91768-6012-485a-b569-a293ea6d48802024-06-24WarningsExact identifier
unii: 15FIX9V2JP
Yves Saint Laurent All Hours Foundation Broad Spectrum SPF 30 Sunscreen Luminous Matte FoundationOCTINOXATE AND TITANIUM DIOXIDEL'Oreal USA Products Inc43539766-2e70-4b42-b64b-1d30367b2eb92024-06-24WarningsExact identifier
unii: 15FIX9V2JP
Exel Clarifying Line SPF 50OCTINOXATE, OCTOCRYLENE, OXYBENZONE, TATANIUM DIOXIDEBiocosmetica Exel Argentina SRLe65a68f6-d1b7-4cbf-a3f8-5cc04036221a2024-06-23WarningsExact identifier
unii: 15FIX9V2JP
ATORVASTATIN CALCIUMATORVASTATIN CALCIUMNuCare Pharmaceuticals,Inc.9e014adf-251e-126e-e053-2995a90a05bf2024-06-20Warnings, Adverse reactionsExact identifier
rxcui: 617310
unii: 48A5M73Z4Q
ATORVASTATIN CALCIUMATORVASTATIN CALCIUMNuCare Pharmaceuticals,Inc.a0835fa8-bd55-33bd-e053-2a95a90a96b12024-06-20Warnings, Adverse reactionsExact identifier
rxcui: 617312
unii: 48A5M73Z4Q
ATORVASTATIN CALCIUMATORVASTATIN CALCIUMNuCare Pharmaceuticals,Inc.a0732bc4-702d-f566-e053-2a95a90a1d692024-06-20Warnings, Adverse reactionsExact identifier
rxcui: 617311
unii: 48A5M73Z4Q
Atorvastatin CalciumATORVASTATIN CALCIUMNuCare Pharmaceuticals,Inc.95729689-8055-45ae-e053-2995a90a919f2024-06-19Warnings, Adverse reactionsExact identifier
rxcui: 617311
unii: 48A5M73Z4Q
Atorvastatin calciumATORVASTATIN CALCIUMNuCare Pharmaceuticals,Inc.8d5b85cf-d8a0-e4d7-e053-2a95a90aad672024-06-18Warnings, Adverse reactionsExact identifier
rxcui: 259255
unii: 48A5M73Z4Q
Atorvastatin CalciumATORVASTATIN CALCIUMNuCare Pharmaceuticals,Inc.8ee8b455-625c-ead6-e053-2a95a90aed292024-06-18Warnings, Adverse reactionsExact identifier
rxcui: 617312
unii: 48A5M73Z4Q
Protectif Fair TintZINC OXIDE AND TITANIUM DIOXIDEDerma Research Group Inc.1a8c8804-1d6b-b5a5-e063-6394a90a12602024-06-18WarningsExact identifier
unii: 15FIX9V2JP
Extra Strength sugar free AntacidCALCIUM CARBONATEAmerisource Bergen541a8e91-9438-4ebd-8bfc-a2674f6a9c4a2024-06-17WarningsExact identifier
unii: H0G9379FGK
ATORVASTATIN CALCIUMATORVASTATIN CALCIUMNuCare Pharmaceuticals,Inc,1adc3c12-1a78-33a0-e063-6294a90a486a2024-06-14Warnings, Adverse reactionsExact identifier
rxcui: 617311
unii: 48A5M73Z4Q
Atorvastatin CalciumATORVASTATIN CALCIUMNuCare Pharmaceuticals,Inc.862f9f27-c645-2d2e-e053-2991aa0a96b92024-06-14Warnings, Adverse reactionsExact identifier
rxcui: 617311
unii: 48A5M73Z4Q
Atorvastatin CalciumATORVASTATIN CALCIUMNuCare Pharmaceuticals,Inc.862f58d1-476c-2c90-e053-2991aa0ab8212024-06-14Warnings, Adverse reactionsExact identifier
rxcui: 617310
unii: 48A5M73Z4Q
Atorvastatin calciumATORVASTATIN CALCIUMNovadoz Pharmaceuticals LLCbc448f40-421c-490f-8c39-fa81355079732024-06-13Warnings, Adverse reactionsExact identifier
rxcui: 617311
rxcui: 617310
rxcui: 259255
rxcui: 617312
unii: 48A5M73Z4Q

Reported adverse events (FAERS/openFDA)#

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