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 | Type |
|---|---|---|---|
| atorvastatin calcium - A-S Medication Solutions | A-S Medication Solutions | 2025-10-21 | HUMAN PRESCRIPTION DRUG LABEL |
| atorvastatin calcium - A-S Medication Solutions | A-S Medication Solutions | 2025-10-21 | HUMAN PRESCRIPTION DRUG LABEL |
| atorvastatin calcium - Zydus Pharmaceuticals USA Inc. | Zydus Lifesciences Limited | Zydus Pharmaceuticals Limited | Zydus Pharmaceuticals USA Inc. | Zydus Lifesciences Limited | Zydus Pharmaceuticals Limited | 2025-05-30 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70710-1775-0 | atorvastatin calcium | 1000 in 1 BOTTLE | TABLET | 1000 | 3 | |
| 70710-1775-5 | atorvastatin calcium | 500 in 1 BOTTLE | TABLET | 500 | 3 | |
| 70710-1775-9 | atorvastatin calcium | 90 in 1 BOTTLE | TABLET | 90 | 3 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 70710-1775 | ATORVASTATIN CALCIUM TABLET [ZYDUS PHARMACEUTICALS USA INC.] | 2 | Current NDC, 3 package rows | 20240618_55ad4a90-d177-4cce-b7ec-cb75067f6c14.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 70710-1775-0 | EA - Each | 70710-1775 | a646afd8-ac06-42ed-8811-b90381c8edfb | 1 | 2024-08-12 |
| 70710-1775-9 | EA - Each | 70710-1775 | e45202fb-a6b5-4ef4-b5d8-2e053d62c668 | 1 | 2024-08-12 |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| PNV Prenatol | MULTIVITAMIN | PureTek Corporation | 583f0194-0306-f31b-e063-6394a90a2a10 | 2026-08-06 | Warnings, Adverse reactions | H0G9379FGK |
| Atorvastatin calcium | ATORVASTATIN CALCIUM | REMEDYREPACK INC. | 5b3c3043-9af6-48eb-8b10-528e58c88e48 | 2026-08-06 | Warnings, Adverse reactions | 617312 48A5M73Z4Q |
| Atorvastatin calcium | ATORVASTATIN CALCIUM | REMEDYREPACK INC. | 51e24220-3374-4e5e-9a8d-4113002c5bed | 2026-08-06 | Warnings, Adverse reactions | 259255 48A5M73Z4Q |
| Atorvastatin calcium | ATORVASTATIN CALCIUM | REMEDYREPACK INC. | b0bbab86-6789-4ffb-8f84-ee91b69fdb34 | 2026-08-06 | Warnings, Adverse reactions | 617310 48A5M73Z4Q |
| EltaMD UV Restore | TITANIUM DIOXIDE, ZINC OXIDE SUNSCREEN | CP Skin Health Group, Inc | 37fee381-ce6b-4949-9a4a-778aa839fb84 | 2026-08-06 | Warnings | 15FIX9V2JP |
| Atorvastatin calcium | ATORVASTATIN CALCIUM | REMEDYREPACK INC. | 9786388d-ac8d-4646-9fe4-b33e8fda86b2 | 2026-08-05 | Warnings, Adverse reactions | 617311 48A5M73Z4Q |
| Luxe Gloss Hydrating Lip Gloss SPF 35-NAKED HONEY | OCTOCRYLENE 8%, OCTISALATE 5%, TITANIUM DIOXIDE 6%, ZINC OXIDE 8% | Lale Cosmetics LLC | 581fb0cd-c55d-d562-e063-6394a90a7f11 | 2026-08-03 | Warnings | 15FIX9V2JP |
| EltaMD UV Active | ZINC OXIDE AND TITANIUM DIOXIDE SUNSCREEN | CP Skin Health Group, Inc | 39d16479-d491-4c19-aa11-674461687c7b | 2026-08-03 | Warnings | 15FIX9V2JP |
| Atorvastatin Calcium | ATORVASTATIN CALCIUM | REMEDYREPACK INC. | 09cb8375-075c-47e8-a4eb-8ac667ed849e | 2026-07-31 | Warnings, Adverse reactions | 617310 48A5M73Z4Q |
| Continuous Correction Cream | TITANIUM DIOXIDE | Baxter of California, LLC | 1cbcc648-f2e1-af60-e063-6294a90ad4bb | 2026-07-31 | Warnings | 15FIX9V2JP |
| Cover Creme | TITANIUM DIOXIDE | Baxter of California | 31f5e8c4-523f-4596-e063-6294a90a6a12 | 2026-07-31 | Warnings | 15FIX9V2JP |
| Atorvastatin Calcium | ATORVASTATIN CALCIUM | Cardinal Health 107, LLC | aee307d6-b3fa-424f-8656-1f30ff413e95 | 2026-07-30 | Warnings, Adverse reactions | 259255 48A5M73Z4Q |
| DUAL ACTION COMPLETE | FAMOTIDINE, CALCIUM CARBONATE AND MAGNESIUM HYDROXIDE | Amazon.com Services LLC | 4e8a936c-b876-4923-ad9e-d23537b5d7cf | 2026-07-28 | Warnings | H0G9379FGK |
| ATORVASTATIN CALCIUM | ATORVASTATIN CALCIUM | Major Pharmaceuticals | e74278b6-31fc-48d4-97b7-ba500e9e15fb | 2026-07-27 | Warnings, Adverse reactions | 617311 259255 |
| TUMS ULTRA | CALCIUM CARBONATE | Haleon US Holdings LLC | 348d3dfa-6a52-4583-96e3-83c4bf2df45b | 2026-07-27 | Warnings | H0G9379FGK |
| Pepcid Complete | FAMOTIDINE, CALCIUM CARBONATE, AND MAGNESIUM HYDROXIDE | Kenvue Brands LLC | a2ef8424-7d80-42b0-a01e-f378f629b2b6 | 2026-07-24 | Warnings | H0G9379FGK |
| ESIKA COLORFIX POLVOS 32H POLVO COMPACTO FACIAL DE ALTA COBERTURA FPS 15 110-C | OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE | BEL STAR S.A. | 575fb2c3-e332-8a3b-e063-6394a90a9fd9 | 2026-07-24 | Warnings | 15FIX9V2JP |
| Atorvastatin Calcium | ATORVASTATIN CALCIUM | Cardinal Health 107, LLC | fbd1c5da-67fb-4412-acb5-4d4c74a43654 | 2026-07-24 | Warnings, Adverse reactions | 259255 48A5M73Z4Q |
| PRENATE Restore | ASCORBIC ACID, CHOLECALCIFEROL, .ALPHA.-TOCOPHEROL ACETATE, DL-, FOLIC ACID, PYRIDOXINE HYDROCHLORIDE, CYANOCOBALAMIN, BIOTIN, CALCIUM CARBONATE, FERROUS FUMARATE, MAGNESIUM OXIDE, LACTIC ACID AND DOCONEXENT | Avion Pharmaceuticals, LLC | 1076ba9a-0168-492f-ba9b-99fa02186092 | 2026-07-23 | Boxed warning, Warnings, Adverse reactions | H0G9379FGK |
| True Coast SPF 50 Mineral Sunscreen | ZINC OXIDE 18%, TITANIUM DIOXIDE 6% | Foshan Sugar Max Cosmetics CO.,Ltd | 5379466d-8d14-5fc2-e063-6394a90abd7e | 2026-07-22 | Warnings | 15FIX9V2JP |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.