NDC codes

FDA NDC Directory
Product NDC (as listed)50090-2093Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50090-2093Add 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 NDC11-digit (billing)PackageCopy
50090-2093-45009020930460 TABLET in 1 BOTTLE (50090-2093-4)Marketed from Oct 12, 2015

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)
Sulindac
Generic name (nonproprietary)
sulindac
Active ingredients
Sulindac — 200 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 072051
Marketing start
Listing expires
Other FDA classes
Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers
Product ID 50090-2093_57459186-a8ac-4d98-a628-c8fc9f383f71SPL ID 57459186-a8ac-4d98-a628-c8fc9f383f71SPL set ID f4985b1b-7e2c-4911-897a-94c337794babRxCUI 198239UNII 184SNS8VUH

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

N450090209304 followed by a unit qualifier and the quantity

Package 50090-2093-04. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Carefully consider the potential benefits and risks of sulindac tablets and other treatment options before deciding to use sulindac tablets. Use the lowest effective dose for the shortest duration consistent with individual patient treatment goals (see WARNINGS ). Sulindac tablets are indicated for acute or long-term use in the relief of signs and symptoms of the following: Osteoarthritis Rheumatoid arthritis* Ankylosing spondylitis Acute painful shoulder (Acute subacromial bursitis/supraspinatus tendinitis) Acute gouty arthritis

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 072051

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

FDA NDC Directory listings under ANDA 072051
ProductStrengthForm · routeLabelerProduct NDC
SulindacSulindac 200 mg/1TabletOralSun Pharmaceutical Industries, Inc.53489-479
SulindacSulindac 200 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-374

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