NDC 72205-002-11 - Rosuvastatin 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
- 72205-002
- Requested NDC
- 72205-002-11
- Package NDCs from labels
- 72205-002-90, 72205-002-99, 72205-002-11, 72205-002-06, 72205-002-05
- Manufacturer
- Novadoz Pharmaceuticals LLC | MSN LABORATORIES PRIVATE LIMITED | MSN Pharmaceuticals Inc.
- Effective date
- 2024-11-28
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Rosuvastatin Calcium | Novadoz Pharmaceuticals LLC | MSN LABORATORIES PRIVATE LIMITED | MSN Pharmaceuticals Inc. | 2024-11-28 | Human Prescription Drug Label |
| Rosuvastatin Calcium - Bryant Ranch Prepack | Bryant Ranch Prepack | 2024-05-17 | HUMAN PRESCRIPTION DRUG LABEL |
| Rosuvastatin Calcium - Preferred Pharmaceuticals Inc. | Preferred Pharmaceuticals Inc. | 2021-09-13 | HUMAN PRESCRIPTION DRUG LABEL |
| Rosuvastatin Calcium - NuCare Pharmaceuticals,Inc. | NuCare Pharmaceuticals,Inc. | 2021-02-17 | HUMAN PRESCRIPTION DRUG LABEL |
| Rosuvastatin Calcium - Proficient Rx LP | Proficient Rx LP | 2020-02-01 | HUMAN PRESCRIPTION DRUG LABEL |
| ROSUVASTATIN CALCIUM - DIRECT RX | DIRECT RX | 2019-04-24 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 72205-002-05 | Rosuvastatin Calcium | 500 in 1 BOTTLE | TABLET, FILM COATED | 500 | 9 | |
| 72205-002-06 | Rosuvastatin Calcium | 100 in 1 CARTON | TABLET, FILM COATED | 100 | 9 | |
| 72205-002-11 | Rosuvastatin Calcium | 10 in 1 BLISTER PACK | TABLET, FILM COATED | 10 | 9 | |
| 72205-002-90 | Rosuvastatin Calcium | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | 9 | |
| 72205-002-99 | Rosuvastatin Calcium | 1000 in 1 BOTTLE | TABLET, FILM COATED | 1000 | 9 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 72205-002-90 | EA - Each | 72205-002 | 4af0a0f0-0336-490b-9b35-43160a602142 | 1 | 2018-09-05 |
| 72205-002-99 | EA - Each | 72205-002 | cba0fd87-ed3f-40c6-a25a-f6a4436124b9 | 1 | 2018-09-05 |
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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.