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 |
|---|---|---|---|---|---|---|
| ATORVASTATIN CALCIUM | ATORVASTATIN CALCIUM | Northwind Health Company, LLC | f32c8a4f-dee9-86a0-e053-2995a90a3388 | 2026-01-01 | Warnings, Adverse reactions | 617312 |
| ATORVASTATIN CALCIUM | ATORVASTATIN CALCIUM | Northwind Health Company, LLC | f76b9e48-3ef7-e15a-e053-6394a90aed58 | 2026-01-01 | Warnings, Adverse reactions | 259255 |
| ATORVASTATIN CALCIUM | ATORVASTATIN CALCIUM | Northwind Health Company, LLC | 0e10adb3-8d3a-412f-ae56-d9b9bed4641f | 2026-01-01 | Warnings, Adverse reactions | 617310 |
| Atorvastatin Calcium | ATORVASTATIN CALCIUM | Northwind Health Company, LLC | c9f55cb6-a41b-dd27-e053-2a95a90aaeb7 | 2026-01-01 | Warnings, Adverse reactions | 617310 48A5M73Z4Q |
| Atorvastatin Calcium | ATORVASTATIN CALCIUM | Northwind Health Company, LLC | f3084cae-db82-4e6f-e053-2995a90aa36a | 2026-01-01 | Warnings, Adverse reactions | 617311 48A5M73Z4Q |
| Atorvastatin Calcium | ATORVASTATIN CALCIUM | Northwind Health Company, LLC | da6b77a5-2093-b7f7-e053-2995a90ab10d | 2026-01-01 | Warnings, Adverse reactions | 259255 48A5M73Z4Q |
| ATORVASTATIN CALCIUM | ATORVASTATIN CALCIUM | Northwind Health Company, LLC | df6233cf-5b4e-5fbe-e053-2a95a90a0a80 | 2026-01-01 | Warnings, Adverse reactions | 617312 48A5M73Z4Q |
| NUTRALOX | CALCIUM CARBONATE | HART Health | 3941b84e-3b4b-46eb-851b-979bac1ae997 | 2025-12-31 | Warnings | H0G9379FGK |
| Youth Glow Vitamin C CC Cream Sunscreen SPF 50 - Fair | OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE | Pur-lisse Beauty, LLC | 47428cd4-fbad-ba7a-e063-6394a90a1c5c | 2025-12-31 | Warnings | 15FIX9V2JP |
| Youth Glow Vitamin C CC Cream Sunscreen SPF 50 - Medium | OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE | Pur-lisse Beauty, LLC | 47433a62-91e0-b031-e063-6294a90a0d49 | 2025-12-31 | Warnings | 15FIX9V2JP |
| Radiant Glow Illuminating BB Cream Sunscreen SPF 30 - Fair | OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE | Pur-lisse Beauty, LLC | 4743b6a9-4d79-1b2b-e063-6394a90a9710 | 2025-12-31 | Warnings | 15FIX9V2JP |
| Radiant Glow Illuminating BB Cream Sunscreen SPF 30 - Light Medium | OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE | Pur-lisse Beauty, LLC | 4744e501-f12a-6d25-e063-6394a90a2574 | 2025-12-31 | Warnings | 15FIX9V2JP |
| Radiant Glow Illuminating BB Cream Sunscreen SPF 30 - Medium | OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE | Pur-lisse Beauty, LLC | 47456bf5-9f6c-e6a5-e063-6294a90a7054 | 2025-12-31 | Warnings | 15FIX9V2JP |
| Radiant Glow Illuminating BB Cream Sunscreen SPF 30 - Tan | OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE | Pur-lisse Beauty, LLC | 4745ab56-abaa-42de-e063-6394a90a6310 | 2025-12-31 | Warnings | 15FIX9V2JP |
| Radiant Glow Illuminating BB Cream Sunscreen SPF 30 - Tan Deep | OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE | Pur-lisse Beauty, LLC | 4745ebec-acb0-77c4-e063-6394a90aee07 | 2025-12-31 | Warnings | 15FIX9V2JP |
| Radiant Glow Illuminating BB Cream Sunscreen SPF 30 - Deep | OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE | Pur-lisse Beauty, LLC | 47461ad3-a11e-2a11-e063-6294a90a0f8f | 2025-12-31 | Warnings | 15FIX9V2JP |
| Sei Bella CC Brightening Creme Light | OCTINOXATE 7.5%, TITANIUM DIOXIDE 5%, ZINC OXIDE 1% | Melaleuca Inc. | 6894b9d9-a5b5-4c98-e053-2991aa0a9ca2 | 2025-12-31 | Warnings | 15FIX9V2JP |
| Sei Bella CC Brightening Creme Fair | OCTINOXATE 7.5%, TITANIUM DIOXIDE 5%, ZINC OXIDE 1% | Melaleuca Inc. | 6892952a-d032-30bf-e053-2a91aa0a3bba | 2025-12-31 | Warnings | 15FIX9V2JP |
| Sei Bella CC Brightening Creme Medium Tan | OCTINOXATE 7.5%, TITANIUM DIOXIDE 5%, ZINC OXIDE 1% | Melaleuca Inc. | 68a4e8b4-36cb-6306-e053-2a91aa0a6d25 | 2025-12-31 | Warnings | 15FIX9V2JP |
| Sei Bella CC Brightening Creme Medium | OCTINOXATE 7.5%, TITANIUM DIOXIDE 5%, ZINC OXIDE 1% | Melaleuca Inc. | 68a4ed34-f492-67a6-e053-2a91aa0a0428 | 2025-12-31 | Warnings | 15FIX9V2JP |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.