NDC 16729-047-01 - 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
- 16729-047
- Requested NDC
- 16729-047-01
- Package NDCs from labels
- 16729-047-10, 16729-047-15, 16729-047-01, 16729-047-16, 16729-047-17
- Manufacturer
- Accord Healthcare Inc. | Intas Pharmaceuticals Limited
- Effective date
- 2025-10-06
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| ATORVASTATIN CALCIUM - Accord Healthcare Inc. | Intas Pharmaceuticals Limited | Accord Healthcare Inc. | Intas Pharmaceuticals Limited | 2025-10-06 | HUMAN PRESCRIPTION DRUG LABEL |
| ATORVASTATIN CALCIUM - A-S Medication Solutions | A-S Medication Solutions | 2022-08-25 | HUMAN PRESCRIPTION DRUG LABEL |
| ATORVASTATIN CALCIUM - Bryant Ranch Prepack | Bryant Ranch Prepack | 2022-02-14 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 16729-047-01 | ATORVASTATIN CALCIUM | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | 13 | |
| 16729-047-10 | ATORVASTATIN CALCIUM | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | 13 | |
| 16729-047-15 | ATORVASTATIN CALCIUM | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | 13 | |
| 16729-047-16 | ATORVASTATIN CALCIUM | 500 in 1 BOTTLE | TABLET, FILM COATED | 500 | 13 | |
| 16729-047-17 | ATORVASTATIN CALCIUM | 1000 in 1 BOTTLE | TABLET, FILM COATED | 1000 | 13 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 16729-047-15 | EA - Each | 16729-047 | 010cdd35-4a9f-46cb-9e88-e9b995a916e4 | 1 | 2021-06-02 |
| 16729-047-16 | EA - Each | 16729-047 | 8309dc33-7ab2-4f21-b01d-ec2dae00361f | 1 | 2018-08-13 |
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 |
|---|---|---|---|---|---|---|
| Genexa Antacid Maximum Strength | CALCIUM CARBONATE | PNP Pharmaceuticals Inc | 27fde2d4-4d49-d995-e063-6394a90ad648 | 2025-08-31 | Warnings | H0G9379FGK |
| Dolce and Gabbana Everlast Foundation SPF 20 33N Deep | OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE | Dolce & Gabbana Beauty S.R.L | e249507c-d536-4c1d-a99d-857ca1e833d8 | 2025-08-29 | Warnings | 15FIX9V2JP |
| Dolce and Gabbana Everlast Foundation SPF 20 32W Medium Deep | OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE | Dolce & Gabbana Beauty S.R.L | ba99edea-bf68-4118-8bb7-ea40322db46a | 2025-08-29 | Warnings | 15FIX9V2JP |
| Dolce and Gabbana Everlast Foundation SPF 20 34W Deep | OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE | Dolce & Gabbana Beauty S.R.L | 3a239897-9850-417f-8c00-e810a52540c1 | 2025-08-29 | Warnings | 15FIX9V2JP |
| Dolce and Gabbana Everlast Foundation SPF 20 36N Deep | OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE | Dolce & Gabbana Beauty S.R.L | c495afc3-6486-4652-b743-958f28eccaca | 2025-08-29 | Warnings | 15FIX9V2JP |
| Dolce and Gabbana Everlast Foundation SPF 20 35W Deep | OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE | Dolce & Gabbana Beauty S.R.L | 5440ed13-b07e-4c81-a407-d9ac68eaa483 | 2025-08-29 | Warnings | 15FIX9V2JP |
| Dolce and Gabbana Everlast Foundation SPF 20 37W Deep | OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE | Dolce & Gabbana Beauty S.R.L | 9b2c4567-fde7-4b76-9988-b2cba2d3747e | 2025-08-29 | Warnings | 15FIX9V2JP |
| CareOne Acid Reducer Complete | FAMOTIDINE, CALCIUM CARBONATE AND MAGNESIUM HYDROXIDE | American Sales Company | 5d4bea42-25d5-4943-b5ed-471eccd36bf8 | 2025-08-29 | Warnings | H0G9379FGK |
| Atorvastatin calcium | ATORVASTATIN CALCIUM | Bryant Ranch Prepack | 00afce9b-48c9-487a-a738-e359c005c707 | 2025-08-28 | Warnings, Adverse reactions | 259255 48A5M73Z4Q |
| D-Cal Kids | CALCIUM CARBONATE | AiPing Pharmaceutical, Inc. | e768b861-1992-1281-e053-2a95a90a64ac | 2025-08-28 | Warnings | H0G9379FGK |
| Exchange Select Calcium Carbonate Antacid Smoothies Extra Strength Assorted Berries | CALCIUM CARBONATE | Army & Air Force Exchange Service | 3d6fbc95-5f83-a2f5-e063-6394a90a42d5 | 2025-08-28 | Warnings | H0G9379FGK |
| CareOne Acid Reducer Complete | FAMOTIDINE, CALCIUM CARBONATE, MAGNESIUM HYDROXIDE | American Sales Company | 19045840-2d25-43af-8c92-f36c8b903b28 | 2025-08-28 | Warnings | H0G9379FGK |
| Ki No Sin | CALCIUM CARBONATE | NPG Bio Pharmaceuticals Co.,Ltd. | 21fa2bad-5b8b-8aac-e063-6394a90a9f49 | 2025-08-27 | Warnings | H0G9379FGK |
| R Cos | CALCIUM CARBONATE | NPG Bio Pharmaceuticals Co.,Ltd. | 21fa767a-1344-5ed9-e063-6394a90a5fe6 | 2025-08-27 | Warnings | H0G9379FGK |
| Na Mi Cal | CALCIUM CARBONATE | NPG Bio Pharmaceuticals Co.,Ltd. | 20cfbcd1-eb13-933c-e063-6294a90a7e59 | 2025-08-27 | Warnings | H0G9379FGK |
| Ki No Sin | CALCIUM CARBONATE | NPG Bio Pharmaceuticals Co.,Ltd. | 20cf8f80-c638-4d94-e063-6294a90a5400 | 2025-08-27 | Warnings | H0G9379FGK |
| PHOFAY Matte Sunscreen Liquid Foundation SPF 30 2 | ENSULIZOLE,HOMOSALATE,OCTINOXATE,TITANIUM DIOXIDE | Hangzhou Jingshen Trading Co., Ltd. | 3d55291c-9d4c-85c3-e063-6394a90af330 | 2025-08-27 | Warnings | 15FIX9V2JP |
| PHOFAY Matte Sunscreen Liquid Foundation SPF 30 3 | ENSULIZOLE ,HOMOSALATE,OCTINOXATE,TITANIUM DIOXIDE | Hangzhou Jingshen Trading Co., Ltd. | 3d565612-ade5-bfb3-e063-6294a90a0c65 | 2025-08-27 | Warnings | 15FIX9V2JP |
| Sun Bum 30 Mineral Tinted Sunscreen Face | TITANIUM DIOXIDE, ZINC OXIDE | Sun Bum, LLC | 3a290aad-7f40-cb10-e063-6394a90a2e69 | 2025-08-27 | Warnings | 15FIX9V2JP |
| ACID REDUCER COMPLETE | FAMOTIDINE, CALCIUM CARBONATE AND MAGNESIUM HYDROXIDE | Safeway | 484ad323-82cf-4157-bacb-236af8210c87 | 2025-08-27 | Warnings | H0G9379FGK |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.