NDC 70710-1775-00 - 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
- 70710-1775-00
- Package NDCs from labels
- 70710-1775-9, 70710-1775-5, 70710-1775-0, 70710-1775-00
- 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 |
|---|---|---|---|---|---|---|
| e l f Camo Semi Matte CC SPF 30 Rich 620 W | ZINC OXIDE, TITANIUM DIOXIDE, HOMOSALATE, OCTISALATE, OCTOCRYLENE | e.l.f. Cosmetics, Inc. | 798eecb3-ff6e-46d1-9053-b40e9cd02e5c | 2025-10-31 | Warnings | 15FIX9V2JP |
| e l f Camo Semi Matte CC SPF 30 Rich 640 W | ZINC OXIDE, TITANIUM DIOXIDE, HOMOSALATE, OCTISALATE, OCTOCRYLENE | e.l.f. Cosmetics, Inc. | cbf949b3-e640-48eb-acf6-fccd6f258865 | 2025-10-31 | Warnings | 15FIX9V2JP |
| e l f Camo Semi Matte CC SPF 30 Rich 650 C | ZINC OXIDE, TITANIUM DIOXIDE, HOMOSALATE, OCTISALATE, OCTOCRYLENE | e.l.f. Cosmetics, Inc. | b8bfad36-54b7-42f3-bb5b-5eda1a10f021 | 2025-10-31 | Warnings | 15FIX9V2JP |
| e l f Camo Semi Matte CC SPF 30 Rich 660 N | ZINC OXIDE, TITANIUM DIOXIDE, HOMOSALATE, OCTISALATE, OCTOCRYLENE | e.l.f. Cosmetics, Inc. | 853100ea-a9dc-43eb-9715-125b543d2be0 | 2025-10-31 | Warnings | 15FIX9V2JP |
| e l f Camo Semi Matte CC SPF 30 Tan 400 W | ZINC OXIDE, TITANIUM DIOXIDE, HOMOSALATE, OCTISALATE, OCTOCRYLENE | e.l.f. Cosmetics, Inc. | e4f2b579-4886-4e20-a527-c033e9d60bf5 | 2025-10-31 | Warnings | 15FIX9V2JP |
| e l f Camo Semi Matte CC SPF 30 Tan 460 W | ZINC OXIDE, TITANIUM DIOXIDE, HOMOSALATE, OCTISALATE, OCTOCRYLENE | e.l.f. Cosmetics, Inc. | 49255019-fa24-4667-b527-ef7189a51f12 | 2025-10-31 | Warnings | 15FIX9V2JP |
| Clove Hill Tinted Mineral Sunscreen SPF 40 | TITANIUM DIOXIDE, ZINC OXIDE | Clove Hill LLC | eb2ff5a7-384f-4379-b149-47c1c8c2291d | 2025-10-30 | Warnings | 15FIX9V2JP |
| Tinted Mineral Lip Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | Clove Hill LLC | a37db64d-8b79-40f4-843f-f38949c5b9d2 | 2025-10-30 | Warnings | 15FIX9V2JP |
| Amlodipine and Atorvastatin | AMLODIPINE AND ATORVASTATIN | Bryant Ranch Prepack | be709711-e7ee-403f-ad43-873761deee37 | 2025-10-30 | Warnings, Adverse reactions | 48A5M73Z4Q |
| MOOYAM Dark Skin Sunscreen | SUNSCREEN | Guangdong Bisutang Biotechnology Co., LTD | 4246e9f1-1c51-d888-e063-6394a90abda0 | 2025-10-29 | Warnings | 15FIX9V2JP |
| Regular Strength Antacid | CALCIUM CARBONATE | SAFEWAY | ce44254f-6e33-4cbd-a609-6a926376efaf | 2025-10-29 | Warnings | H0G9379FGK |
| Extra Strength | CALCIUM CARBONATE | BETTER LIVING BRANDS, LLC | 9b311b76-1892-4b74-a07a-8b321436d4a0 | 2025-10-29 | Warnings | H0G9379FGK |
| Extra Strength | ANTACID TABLETS | SAFEWAY | f91aa7da-8bdc-4fd2-a9de-fef21674e515 | 2025-10-29 | Warnings | H0G9379FGK |
| Extra Strength Smooth | CALCIUM CARBONATE | SAFEWAY | 4314ac58-03aa-479c-a711-4818cc332531 | 2025-10-29 | Warnings | H0G9379FGK |
| Extra Strength | ANTACID TABLETS | SAFEWAY | 5bdb868d-016d-4175-9283-86c5b77bb26e | 2025-10-29 | Warnings | H0G9379FGK |
| Extra Strength | ANTACID TABLETS | SAFEWAY | 03853f03-081d-4a78-b383-66ac9754d46f | 2025-10-29 | Warnings | H0G9379FGK |
| Ultra Strength | CALCIUM CARBONATE | BETTER LIVING BRANDS LLC | 3ff92c9a-987f-468e-9e18-1e3e171ede14 | 2025-10-29 | Warnings | H0G9379FGK |
| Ultra Strength | CALCIUM CARBONATE | BETTER LIVING BRANDS LLC | 35b3d9d0-b04d-4f6d-b99d-435233803d4b | 2025-10-29 | Warnings | H0G9379FGK |
| Ultra Strength | ANTACID TABLETS | SAFEWAY | 4c6cdd81-5145-4a1f-888f-85cf5d856c39 | 2025-10-29 | Warnings | H0G9379FGK |
| Extra Strength Smooth | ANTACID TABLETS | SAFEWAY | 8ed35c3b-9878-4889-90f7-a3973cf806e0 | 2025-10-29 | Warnings | H0G9379FGK |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.