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 |
|---|---|---|---|---|---|---|
| ANESSA PERFECT UV SUNSCREEN SKINCARE MILK GB | ZINC OXIDE OCTOCRYLENE ETHYLHEXYL SALICYLATE HOMOSALATE TITANIUM DIOXIDE | HONGKONG JIAHE INTERNATIONAL HOLDING LIMITED | 5354af18-50c4-5fba-e063-6394a90ace39 | 2026-06-03 | Warnings | 15FIX9V2JP |
| Rohto Digi-Eye | HYPROMELLOSE, TETRAHYDROZOLINE HYDROCHLORIDE | The Mentholatum Company | 5d6f37b9-b568-4cb6-92de-eb40779f3f8c | 2026-06-03 | Warnings | 3NXW29V3WO |
| Vitalux | MULTIVITAMIN | PureTek Corporation | 52d5eee7-8146-cc62-e063-6394a90a8c3f | 2026-06-02 | Boxed warning, Adverse reactions | H0G9379FGK |
| ATOMY BB SUNSCREEN | TITANIUM DIOXIDE, ZINC OXIDE | ATOMY CO., LTD. | b0cd27ee-4917-4800-bcdf-c6e14b28c1d1 | 2026-06-02 | Warnings | 15FIX9V2JP |
| Atomy Sunscreen White Broad Spectrum SPF 50 PLUS | HOMOSALATE, OCTISALATE, TITANIUM DIOXIDE, ZINC OXIDE | ATOMY CO., LTD. | ad0b9091-a990-45bf-93f4-d886be1bbffe | 2026-06-02 | Warnings | 15FIX9V2JP |
| Atomy Sunscreen Beige Broad Spectrum SPF 50 PLUS | HOMOSALATE, OCTISALATE, TITANIUM DIOXIDE, ZINC OXIDE | ATOMY CO., LTD. | 994d5680-284e-4faf-a29b-4d28f8d46e8f | 2026-06-02 | Warnings | 15FIX9V2JP |
| Antacid- Calcium Carbonate | CALCIUM CARBONATE | Anhui Jiuhe Health Industry Co., Ltd | 53518897-5387-38cf-e063-6394a90aa3e1 | 2026-06-02 | Warnings | H0G9379FGK |
| Matte Veil Tinted Broad Spectrum Sunscreen SPF 40 | ZINC OXIDE, TITANIUM DIOXIDE | Private Label Skin Care | a8d60212-18a7-42af-8bb3-bfcff7690a49 | 2026-06-02 | Warnings | 15FIX9V2JP |
| The Mineral Melt SPF30 | ZINC OXIDE, TITANIUM DIOXIDE | Dune Suncare Inc. | 2114fc3b-c8ce-45d2-8a82-4dc54f0adaf3 | 2026-06-02 | Warnings | 15FIX9V2JP |
| Good Neighbor Pharmacy Dual Action Complete | FAMOTIDINE, CALCIUM CARBONATE AND MAGNESIUM HYDROXIDE | Amerisource Bergen | b7453c0e-b452-409b-a324-83fdd105bfd0 | 2026-06-02 | Warnings | H0G9379FGK |
| LA ROCHE POSAY LABORATOIRE DERMATOLOGIQUE ANTHELIOS UV AIR MINERAL SERUM SUNSCREEN BROAD SPECTRUM SPF 50 | TITANIUM DIOXIDE AND ZINC OXIDE | LOreal USA Products Inc | a1acb789-5bf4-4447-b3c5-4a7d4d3013a7 | 2026-06-01 | Warnings | 15FIX9V2JP |
| Pepcid Complete | FAMOTIDINE, CALCIUM CARBONATE, AND MAGNESIUM HYDROXIDE | Savings Distributors LLC | 549136d5-8f2c-d417-e063-6394a90a23e4 | 2026-06-01 | Warnings | H0G9379FGK |
| Regular Strength Antacid Peppermint | CALCIUM CARBONATE | Hyvee Inc | 4e5526a8-d9ad-965b-e063-6294a90a8333 | 2026-06-01 | Warnings | H0G9379FGK |
| Dual Action Complete | FAMOTIDINE, CALCIUM CARBONATE, MAGNESIUM HYDROXIDE | Meijer Distribution Inc | 50fe57e1-6678-4697-9b35-4673db67d4fb | 2026-06-01 | Warnings | H0G9379FGK |
| KIEHLS DERMATOLOGIST SOLUTIONS BETTER SCREEN MINER ALL UV SERUM BROAD SPECTRUM SPF 50 PLUS MINERAL SUNSCREEN | TITANIUM DIOXIDE AND ZINC OXIDE | LOreal USA Products Inc | 294e6049-12b5-4b45-ae00-8ee1d9d2a1a4 | 2026-05-29 | Warnings | 15FIX9V2JP |
| Atorvastatin calcium | ATORVASTATIN CALCIUM | NuCare Pharmaceuticals, Inc. | 52f99e39-fb92-e9f5-e063-6294a90a1b6a | 2026-05-29 | Warnings, Adverse reactions | 617310 48A5M73Z4Q |
| ATORVASTATIN CALCIUM | ATORVASTATIN CALCIUM | Cardinal Health 107, LLC | 75ea68e0-12e2-4e27-876f-f24f6e33a0b7 | 2026-05-29 | Warnings, Adverse reactions | 617311 259255 |
| O HUI DAY SHIELD PERFECT SUN BLACK BROAD SPECTRUM SPF 50 SUNSCREEN | OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE | LG H&H Co., Ltd. | 52ba9423-8b9b-38f7-e063-6394a90a95da | 2026-05-26 | Warnings | 15FIX9V2JP |
| Mineral SPF 30 Moisturizer | MINERAL SPF 30 MOISTURIZER | Dont Run Out Inc (DBA: Public Goods) | 52462e7e-0c2c-6b64-e063-6394a90a4230 | 2026-05-21 | Warnings | 15FIX9V2JP |
| Atorvastatin Calcium | ATORVASTATIN CALCIUM | Coupler LLC | 52561b3e-c20f-3536-e063-6394a90a6198 | 2026-05-21 | Warnings, Adverse reactions | 617312 48A5M73Z4Q |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.