What is NDC 50090-0975?

50090-0975 is the product NDC for Pravastatin Sodium, Pravastatin sodium 20 mg/1 tablet, listed with the FDA by A-S Medication Solutions. It has 2 package NDCs, shown above in 10- and 11-digit form.

A-S Medication Solutions, NDC labeler code 50090. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Pravastatin Sodium?

184 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Pravastatin Sodium NDC 50090-0975 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)50090-0975Labeler and product segments. Claims need a package NDC.

Product NDC at billing width50090-0975Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
50090-0975-0	5009009750050090097500	30 TABLET in 1 BOTTLE (50090-0975-0)Marketed from Nov 28, 2014
50090-0975-1	5009009750150090097501	90 TABLET in 1 BOTTLE (50090-0975-1)Marketed from Nov 28, 2014

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Pravastatin Sodium
Generic name (nonproprietary): pravastatin sodium
Active ingredients: Pravastatin sodium — 20 mg/1
Dosage form: Tablet
Route: Oral
Labeler: A-S Medication SolutionsNDC labeler code 50090
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 077987
Marketing start: May 11, 2007
Listing expires: Dec 31, 2026
Other FDA classes: Hydroxymethylglutaryl-CoA Reductase Inhibitors (Mechanism)
Identifiers: Product ID 50090-0975_e0a2b342-26bb-4c86-b9c4-20fc5160c98fSPL ID e0a2b342-26bb-4c86-b9c4-20fc5160c98fSPL set ID a75de063-c751-4647-bb9e-d4050c1e31fcRxCUI 904467UNII 3M8608UQ61
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

N450090097500 followed by a unit qualifier and the quantity

Package 50090-0975-00. 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

Current FDA label (SPL), effective Dec 14, 2023.

Indications (excerpt from the label)

Pravastatin sodium tablets are indicated: 1. To reduce the risk of myocardial infarction, myocardial revascularization procedures, and cardiovascular mortality in adults with elevated low-density lipoprotein cholesterol (LDL-C) without clinically evident coronary heart disease (CHD). 2. To reduce the risk of coronary death, myocardial infarction, myocardial revascularization procedures, stroke or transient ischemic attack, and slow the progression of coronary atherosclerosis in adults with clinically evident CHD. 3. As an adjunct to diet to reduce LDL-C in adults with primary hyperlipidemia. 4. As an adjunct to diet to reduce LDL-C in pediatric patients ages 8 years and older with heterozygo…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 50090-0975

What is NDC 50090-0975?: 50090-0975 is the product NDC for Pravastatin Sodium, Pravastatin sodium 20 mg/1 tablet, listed with the FDA by A-S Medication Solutions. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Pravastatin Sodium.
What is the active ingredient?: Pravastatin sodium.
Who is the labeler?: A-S Medication Solutions, NDC labeler code 50090. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Pravastatin Sodium?: 184 other product NDCs are listed under this name. See all Pravastatin Sodium NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Pravastatin Sodium NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Pravastatin Sodium	Pravastatin sodium 30 mg/1	TabletOral	Havix Group Inc d-b-a Aavis Pharmaceuticals	71337-289	71337-0289-09
Pravastatin Sodium	Pravastatin sodium 60 mg/1	TabletOral	Havix Group Inc d-b-a Aavis Pharmaceuticals	71337-290	71337-0290-09
Pravastatin sodium	Pravastatin sodium 80 mg/1	TabletOral	Aurobindo Pharma Limited	84386-167	84386-0167-9084386-0167-99
Pravastatin Sodium	Pravastatin sodium 10 mg/1	TabletOral	Amici Pharma, Inc.	69292-101	69292-0101-1069292-0101-5069292-0101-90
Pravastatin Sodium	Pravastatin sodium 20 mg/1	TabletOral	Amici Pharma, Inc.	69292-102	69292-0102-1069292-0102-5069292-0102-90
Pravastatin Sodium	Pravastatin sodium 40 mg/1	TabletOral	Amici Pharma, Inc.	69292-103	69292-0103-1069292-0103-5069292-0103-90
Pravastatin Sodium	Pravastatin sodium 80 mg/1	TabletOral	Amici Pharma, Inc.	69292-104	69292-0104-1069292-0104-5069292-0104-90
Pravastatin Sodium	Pravastatin sodium 10 mg/1	TabletOral	Northwind Health Company, LLC	82868-104	82868-0104-30
Pravastatin sodium	Pravastatin sodium 20 mg/1	TabletOral	Safecor Health LLC	48433-148	48433-0148-20
Pravastatin sodium	Pravastatin sodium 40 mg/1	TabletOral	Safecor Health LLC	48433-149	48433-0149-20

All 185 Pravastatin Sodium NDCs

Other NDCs under ANDA 077987

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

FDA NDC Directory listings under ANDA 077987
Product	Strength	Form · route	Labeler	Product NDC
Pravastatin Sodium	Pravastatin sodium 40 mg/1	TabletOral	A-S Medication Solutions	50090-1533
Pravastatin Sodium	Pravastatin sodium 10 mg/1	TabletOral	A-S Medication Solutions	50090-1594
Pravastatin Sodium	Pravastatin sodium 80 mg/1	TabletOral	A-S Medication Solutions	50090-5809
Pravastatin Sodium	Pravastatin sodium 20 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-8421
Pravastatin Sodium	Pravastatin sodium 10 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-8425
Pravastatin Sodium	Pravastatin sodium 20 mg/1	TabletOral	A-S Medication Solutions	50090-7709
Pravastatin Sodium	Pravastatin sodium 20 mg/1	TabletOral	A-S Medication Solutions	50090-7710
Pravastatin Sodium	Pravastatin sodium 10 mg/1	TabletOral	American Health Packaging	60687-886
Pravastatin Sodium	Pravastatin sodium 10 mg/1	TabletOral	CIPLA USA INC.	69097-788
Pravastatin Sodium	Pravastatin sodium 20 mg/1	TabletOral	CIPLA USA INC.	69097-789
Pravastatin Sodium	Pravastatin sodium 40 mg/1	TabletOral	CIPLA USA INC.	69097-791
Pravastatin Sodium	Pravastatin sodium 80 mg/1	TabletOral	CIPLA USA INC.	69097-792
Pravastatin Sodium	Pravastatin sodium 20 mg/1	TabletOral	NCS HealthCare of KY, LLC dba Vangard Labs	0615-8540
Pravastatin Sodium	Pravastatin sodium 20 mg/1	TabletOral	American Health Packaging	60687-897
Pravastatin Sodium	Pravastatin sodium 10 mg/1	TabletOral	Coupler LLC	67046-1518
Pravastatin Sodium	Pravastatin sodium 20 mg/1	TabletOral	Coupler LLC	67046-1519
Pravastatin Sodium	Pravastatin sodium 40 mg/1	TabletOral	American Health Packaging	60687-908
Pravastatin Sodium	Pravastatin sodium 40 mg/1	TabletOral	NCS HealthCare of KY, LLC dba Vangard Labs	0615-8541
Pravastatin Sodium	Pravastatin sodium 80 mg/1	TabletOral	NCS HealthCare of KY, LLC dba Vangard Labs	0615-8542
Pravastatin Sodium	Pravastatin sodium 40 mg/1	TabletOral	Northwind Health Company, LLC	51655-594

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