Rosuvastatin Calcium NDC 60687-256

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

American Health Packaging

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 079170

Marketing start

Sep 21, 2016

Listing expires

Dec 31, 2026

Other FDA classes

Hydroxymethylglutaryl-CoA Reductase Inhibitors (Mechanism)

Identifiers

Product ID 60687-256_401aadf4-8665-4427-e063-6394a90a7820SPL ID 401aadf4-8665-4427-e063-6394a90a7820SPL set ID b7491a1a-570e-40ea-b65b-f956c9e284a6RxCUI 859424, 859747, 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

N460687025601 followed by a unit qualifier and the quantity Copy

Package 60687-0256-01. 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 079170

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

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