NDC 43598-830-79 - 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
- 43598-830
- Requested NDC
- 43598-830-79
- Package NDCs from labels
- 43598-830-90, 43598-830-05, 43598-830-79, 43598-830-78
- Manufacturer
- Preferred Pharmaceuticals Inc.
- Effective date
- 2025-01-03
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Atorvastatin Calcium - Preferred Pharmaceuticals Inc. | Preferred Pharmaceuticals Inc. | 2025-01-03 | HUMAN PRESCRIPTION DRUG LABEL |
| Atorvastatin Calcium - Dr. Reddy's Laboratories Inc | Dr. Reddy's Laboratories Limited FTO-Sez-Process Unit-01 | Dr. Reddy's Laboratories Inc | Dr. Reddy's Laboratories Limited FTO-Sez-Process Unit-01 | 2024-04-24 | HUMAN PRESCRIPTION DRUG LABEL |
| CALCIUM CARBONATE - NuCare Pharmaceuticals,Inc. | NuCare Pharmaceuticals,Inc.. | NuCare Pharmaceuticals,Inc. | NuCare Pharmaceuticals,Inc.. | 2023-09-20 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 43598-830-05 | Atorvastatin Calcium | 500 in 1 BOTTLE | TABLET | 500 | 8 | |
| 43598-830-78 | Atorvastatin Calcium | 10 in 1 CARTON | TABLET | 10 | 8 | |
| 43598-830-79 | Atorvastatin Calcium | 10 in 1 BLISTER PACK | TABLET | 10 | 8 | |
| 43598-830-90 | Atorvastatin Calcium | 90 in 1 BOTTLE | TABLET | 90 | 8 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 43598-830-05 | EA - Each | 43598-830 | 56542fcb-accf-4a72-b166-13403f16e151 | 1 | 2022-11-07 |
| 43598-830-90 | EA - Each | 43598-830 | 8b1fcd50-f665-411a-ace5-7273ad26dc57 | 1 | 2022-11-07 |
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 |
|---|---|---|---|---|---|---|
| Dolce and Gabbana Everlast Foundation SPF 20 05N Light | OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE | Dolce & Gabbana Beauty S.R.L | f93aa5d2-90ab-4e11-874e-2ede4b25c4b6 | 2025-08-04 | Warnings | 15FIX9V2JP |
| Dolce and Gabbana Everlast Foundation SPF 20 04C Light | OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE | Dolce & Gabbana Beauty S.R.L | f055cd51-7b1d-43df-8990-8f60ba1eb91c | 2025-08-04 | Warnings | 15FIX9V2JP |
| Dolce and Gabbana Everlast Foundation SPF 20 07N Light | OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE | Dolce & Gabbana Beauty S.R.L | d4c76bc5-205b-45fd-8a02-4f4b17458503 | 2025-08-04 | Warnings | 15FIX9V2JP |
| Atorvastatin Calcium | ATORVASTATIN CALCIUM | Teva Pharmaceuticals, Inc. | d3497ad6-b549-4144-b57f-b2088ad80b09 | 2025-08-01 | Warnings, Adverse reactions | 617311 617310 259255 617312 48A5M73Z4Q |
| ATORVASTATIN CALCIUM | ATORVASTATIN CALCIUM | Camber Pharmaceuticals, Inc. | 25c8f92f-9cb6-482b-82e1-16ad7c94e7b3 | 2025-07-28 | Warnings, Adverse reactions | 617311 617310 259255 617312 48A5M73Z4Q |
| Neutrogena Mineral Invisible Daily Defense Face Sunscreen Broad Spectrum SPF 30 | TITANIUM DIOXIDE, ZINC OXIDE | Kenvue Brands LLC | 003123d2-9675-fdd2-e063-6294a90a0130 | 2025-07-28 | Warnings | 15FIX9V2JP |
| Neutrogena Mineral Ultra Sheer Face SPF 70 | TITANIUM DIOXIDE, ZINC OXIDE | Kenvue Brands LLC | 20e0badf-fe25-1d27-e063-6294a90a7cfe | 2025-07-28 | Warnings | 15FIX9V2JP |
| Dolce and Gabbana Everlast Foundation SPF 20 01N Light | OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE | Dolce & Gabbana Beauty S.R.L | 2ccf4e45-4cec-417d-9f4c-28f376025f1d | 2025-07-25 | Warnings | 15FIX9V2JP |
| Sunscreen | TITANIUM DIOXIDE 6.8% | Baxter of California, LLC | 146030bc-2bf4-25ea-e063-6294a90a4613 | 2025-07-24 | Warnings | 15FIX9V2JP |
| La Defense Broad Spectrum SPF 30 Mineral Sunscreen | ZINC OXIDE, TITANIUM DIOXIDE | Luzern Laboratories, Inc | 3f00befa-415d-415d-89e1-6ba8770ba51e | 2025-07-21 | Warnings | 15FIX9V2JP |
| Atorvastatin Calcium | ATORVASTATIN CALCIUM | Mylan Institutional Inc. | 7c1083b9-7a20-475d-ba12-4f5d0b53e601 | 2025-07-18 | Warnings, Adverse reactions | 617311 617310 259255 617312 48A5M73Z4Q |
| Gas-X Total Relief Maximum Strength | CALCIUM CARBONATE, SIMETHICONE | Haleon US Holdings LLC | edb0f11a-bdb7-484d-9257-09ff47b0fca4 | 2025-07-15 | Warnings | H0G9379FGK |
| Amarte ULTRA VEIL Daily | SUNSCREEN | Amarte USA LLC | 39e9ca98-d0e8-6b8f-e063-6394a90aa366 | 2025-07-15 | Warnings | 15FIX9V2JP |
| Amarte ULTRA VEIL BB Fair | SUNSCREEN | Amarte USA LLC | 39e87950-4103-c2eb-e063-6394a90a0552 | 2025-07-15 | Warnings | 15FIX9V2JP |
| leader acid reducer complete | FAMOTIDINE, CALCIUM CARBONATE, MAGNESIUM HYDROXIDE | Cardinal Health 110, LLC. dba Leader | 6a492dd2-61f1-4020-bebd-fcc8e5647207 | 2025-07-08 | Warnings | H0G9379FGK |
| Dual Action Complete | FAMOTIDINE, CALCIUM CARBONATE, MAGNESIUM HYDROXIDE | Kroger Company | bf2fcb88-418f-4d5d-85ba-ec165a53ab04 | 2025-07-07 | Warnings | H0G9379FGK |
| MGC Health Antacid Soft Chews Cherry Flavor | CALCIUM CARBONATE | Xiamen Kang Zhongyuan Biotechnology Co., Ltd. | 3958ec0a-8f32-6918-e063-6294a90ac1c4 | 2025-07-07 | Warnings | H0G9379FGK |
| ATORVASTATIN CALCIUM | ATORVASTATIN CALCIUM | NuCare Pharmaceuticals, Inc. | 395dbb88-5889-c91c-e063-6394a90a8daf | 2025-07-07 | Warnings, Adverse reactions | 259255 48A5M73Z4Q |
| Equate Acid Reducer Complete | FAMOTIDINE, CALCIUM CARBONATE, MAGNESIUM HYDROXIDE | Wal-Mart Stores Inc | cb683c1c-db81-40a9-9ec5-f8dfa0dcf812 | 2025-07-07 | Warnings | H0G9379FGK |
| Dual Action Complete | FAMOTIDINE, CALCIUM CARBONATE, MAGNESIUM HYDROXIDE | H E B | ea712fc4-7f27-4556-b1b8-028f3f6ce57a | 2025-07-07 | Warnings | H0G9379FGK |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.