Rosuvastatin Calcium NDC 68788-7612

Product information

Brand name (proprietary)

Rosuvastatin Calcium

Generic name (nonproprietary)

rosuvastatin calcium

Active ingredients

Rosuvastatin calcium — 20 mg/1

Dosage form

Tablet, Film coated

Route

Oral

Labeler

Preferred Pharmaceuticals, Inc.

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 208898

Marketing start

Jun 1, 2020

Listing expires

Dec 31, 2027

Other FDA classes

Hydroxymethylglutaryl-CoA Reductase Inhibitors (Mechanism)

Identifiers

Product ID 68788-7612_5f979f26-fe2b-4e7c-931c-2a627c46c201SPL ID 5f979f26-fe2b-4e7c-931c-2a627c46c201SPL set ID 6ef51f7c-2899-4b09-bf8b-09e5b4ac3424RxCUI 859751UNII 83MVU38M7Q

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

N468788761202 followed by a unit qualifier and the quantity Copy

Package 68788-7612-02. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 208898

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

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