NDC codes

FDA NDC Directory
Product NDC (as listed)50090-7642Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50090-7642Add 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
50090-7642-0500907642008 TABLET in 1 BOTTLE (50090-7642-0)Marketed from Aug 26, 2025

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)
Cabergoline
Generic name (nonproprietary)
cabergoline
Active ingredients
Cabergoline — .5 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 218618
Marketing start
Listing expires
Other FDA classes
Ergolines (Chemical structure)
Identifiers
Product ID 50090-7642_f0d4a3cf-7de2-4959-b8b6-a2753d0deb15SPL ID f0d4a3cf-7de2-4959-b8b6-a2753d0deb15SPL set ID 9405c116-4a77-4e14-9ab8-25e899595cdfRxCUI 199703UNII LL60K9J05T
Pharmacologic class
Ergot Derivative

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

N450090764200 followed by a unit qualifier and the quantity

Package 50090-7642-00. 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 .

Indications (excerpt from the label)

INDICATIONS AND USAGE Cabergoline tablets are indicated for the treatment of hyperprolactinemic disorders, either idiopathic or due to pituitary adenomas.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 218618

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

FDA NDC Directory listings under ANDA 218618
ProductStrengthForm · routeLabelerProduct NDC
CabergolineCabergoline .5 mg/1TabletOralAmneal Pharmaceuticals NY LLC69238-2693

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