Rosuvastatin Calcium NDC 70518-4697

Product information

Brand name (proprietary)

Rosuvastatin Calcium

Generic name (nonproprietary)

rosuvastatin calcium

Active ingredients

Rosuvastatin calcium — 5 mg/1

Dosage form

Tablet

Route

Oral

Labeler

REMEDYREPACK INC.

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 207626

Marketing start

Jul 12, 2026

Listing expires

Dec 31, 2027

Other FDA classes

Hydroxymethylglutaryl-CoA Reductase Inhibitors (Mechanism)

Identifiers

Product ID 70518-4697_5bffb83d-ea01-1eeb-e063-6394a90acd41SPL ID 5bffb83d-ea01-1eeb-e063-6394a90acd41

Pharmacologic class

HMG-CoA Reductase Inhibitor

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N470518469700 followed by a unit qualifier and the quantity Copy

Package 70518-4697-00. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

The FDA listing for this product does not reference a label (SPL) set.

Other NDCs under ANDA 207626

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

Showing 20 of 22.