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 |
|---|---|---|---|---|---|---|
| SPF30 SUMMER BLEND SUNSCREEN | TITANIUM DIOXIDE | ORGANIC & SUSTAINABLE BEAUTY | 9641b71a-81f2-4157-801b-162188392a91 | 2024-11-07 | Warnings | 15FIX9V2JP |
| SPF30 SUPER SENSITIVE SUNSCREEN | TITANIUM DIOXIDE | ORGANIC & SUSTAINABLE BEAUTY | d79cf2d9-4923-452a-bb44-67e059ee37ee | 2024-11-07 | Warnings | 15FIX9V2JP |
| SPF30 EVERYDAY/YEAR-ROUND SUNSCREEN | TITANIUM DIOXIDE | ORGANIC & SUSTAINABLE BEAUTY | d4f30d95-4a3f-49ad-817e-faa86fca5018 | 2024-11-07 | Warnings | 15FIX9V2JP |
| SPF30 CALENDULA SUNSCREEN | TITANIUM DIOXIDE | ORGANIC & SUSTAINABLE BEAUTY | 64580be7-868c-40fb-b7b8-840b417b25d3 | 2024-11-06 | Warnings | 15FIX9V2JP |
| KIDS SPF30 SUPER SENSITIVE PLUS C111 SUNSCREEN | TITANIUM DIOXIDE | ORGANIC & SUSTAINABLE BEAUTY | 20ebe264-2f79-4eef-b83d-3f09a3ca2898 | 2024-11-06 | Warnings | 15FIX9V2JP |
| Cream Oil Sunscreen | ZINC OXIDE, TITANIUM DIOXIDE SUNSCREEN | Owen Biosciences, Inc. | b2ccdfea-1c27-42af-b9d8-752e9f91ae87 | 2024-11-05 | Warnings | 15FIX9V2JP |
| ATORVASTATIN CALCIUM | ATORVASTATIN CALCIUM | Proficient Rx LP | 4b2d0de1-50f0-4356-aa79-88696be8ac3d | 2024-11-01 | Warnings, Adverse reactions | 617310 48A5M73Z4Q |
| ATORVASTATIN CALCIUM | ATORVASTATIN CALCIUM | Bryant Ranch Prepack | 76e8e69c-590f-4f74-82e1-199d8d14fa80 | 2024-11-01 | Warnings, Adverse reactions | 617311 48A5M73Z4Q |
| ATORVASTATIN CALCIUM | ATORVASTATIN CALCIUM | Proficient Rx LP | 5a132b72-5318-43ab-881d-a2e51bd20bdc | 2024-11-01 | Warnings, Adverse reactions | 617312 48A5M73Z4Q |
| ATORVASTATIN CALCIUM | ATORVASTATIN CALCIUM | Bryant Ranch Prepack | 1fb2d51e-360c-40a3-8072-f22893890a51 | 2024-10-31 | Warnings, Adverse reactions | 617311 48A5M73Z4Q |
| Addiclenz | BOLDO, CARDUUS MARIANUS, CHELIDONIUM MAJUS, PETROSELINUM SATIVUM, TARAXACUM OFFICINALE, ARSENICUM ALBUM, BISPHENOL A, COBALTUM METALLICUM, CUPRUM METALLICUM, GLYPHOSATE, IODIUM, LYCOPODIUM CLAVATUM, PHOSPHORICUM ACIDUM, SELENIUM METALLICUM, ZINCUM METALLICUM, ASPARTAME, BENZALKONIUM CHLORIDE, FORMALINUM, METHYLENE CHLORIDE, METHYL PARABEN, PROPYL PARABEN, SODIUM BENZOATE, SODIUM CITRATE, TITANIUM DIOXIDE, ZINCUM OXYDATUM | Deseret Biologicals, Inc. | 8a3b75ca-8fec-4318-8a55-8bde0b82637d | 2024-10-31 | Warnings | 15FIX9V2JP |
| ATORVASTATIN CALCIUM | ATORVASTATIN CALCIUM | Bryant Ranch Prepack | cbeb2aa0-24a2-430f-b456-34a4e63e1817 | 2024-10-31 | Warnings, Adverse reactions | 617310 48A5M73Z4Q |
| ATORVASTATIN CALCIUM | ATORVASTATIN CALCIUM | Bryant Ranch Prepack | ace2c37e-b525-4fe7-8316-9bd3fa4a092c | 2024-10-31 | Warnings, Adverse reactions | 617312 48A5M73Z4Q |
| RITE AID Pharmacy Ultra Strength Assorted Fruits | CALCIUM CARBONATE | RITE AID CORPORATION | 2989649c-e5ab-4118-a4d4-0f22a7f9f0a0 | 2024-10-30 | Warnings | H0G9379FGK |
| Kids Antacid | CALCIUM CARBONATE | RITE AID CORPORATION | 9255322d-dd0d-4429-b1ca-805c7348c38d | 2024-10-30 | Warnings | H0G9379FGK |
| Extra Strength Smooth Antacid | CALCIUM CARBONATE | RITE AID CORPORATION | 23fa3378-d9f9-4671-ba1c-9c9611b1fbef | 2024-10-30 | Warnings | H0G9379FGK |
| Rite Aid Extra Strength Assorted Fruit | CALCIUM CARBONATE | RITE AID CORPORATION | d405655a-260d-4a26-bf6f-053c6a6c87af | 2024-10-30 | Warnings | H0G9379FGK |
| Extra Strength Antacid | CALCIUM CARBONATE | RITE AID CORPORATION | c6bbffbc-2d00-4a5c-80aa-5e59204cca9f | 2024-10-30 | Warnings | H0G9379FGK |
| Rite Aid Extra Strength Assorted Fruits | CALCIUM CARBONATE | RITE AID CORPORATION | 60d5fa96-528e-486c-ada2-cdfef090b61a | 2024-10-30 | Warnings | H0G9379FGK |
| Rite Aid Ultra Strength Peppermint Flavor | CALCIUM CARBONATE | RITE AID CORPORATION | 4e963099-fd7f-4862-9f9c-9f1fb963779e | 2024-10-30 | Warnings | H0G9379FGK |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.