NDC codes

FDA NDC Directory
Product NDC (as listed)55289-119Labeler and product segments. Claims need a package NDC.
Product NDC at billing width55289-0119Add 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
55289-119-02552890119022 SUPPOSITORY in 1 BOTTLE, PLASTIC (55289-119-02)Marketed from Dec 22, 2010
55289-119-06552890119066 SUPPOSITORY in 1 BOTTLE, PLASTIC (55289-119-06)Marketed from Jan 18, 2023

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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)
Compro
Generic name (nonproprietary)
prochlorperazine
Active ingredients
Prochlorperazine — 25 mg/1
Dosage form
Suppository
Route
Rectal
Labeler
PD-Rx Pharmaceuticals, Inc.NDC labeler code 55289
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 040246
Marketing start
Listing expires
Other FDA classes
Phenothiazines (Chemical structure)
Identifiers
Product ID 55289-119_30c7c9fd-e624-97a7-e063-6294a90ad3a7SPL ID 30c7c9fd-e624-97a7-e063-6294a90ad3a7SPL set ID b23b67eb-78b7-48eb-84ff-c95d3ce8683cRxCUI 198159, 284254UNII YHP6YLT61TUPC 0355289119029
Pharmacologic class
Phenothiazine

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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

NDC on a medical claim

N455289011902 followed by a unit qualifier and the quantity

Package 55289-0119-02. 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

Current FDA label (SPL), effective . This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Prochlorperazine 25 mg suppositories are indicated in the control of severe nausea and vomiting in adults.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 55289-119

What is NDC 55289-119?
55289-119 is the product NDC for Compro (prochlorperazine), Prochlorperazine 25 mg/1 suppository, listed with the FDA by PD-Rx Pharmaceuticals, Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Compro (Prochlorperazine).
What is the active ingredient?
Prochlorperazine.
Who is the labeler?
PD-Rx Pharmaceuticals, Inc., NDC labeler code 55289. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Compro?
1 other product NDC are listed under this name. See all Compro 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 Compro NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
ComproprochlorperazineProchlorperazine 25 mg/1SuppositoryRectalPadagis US LLC0574-722600574-7226-12

Other NDCs under ANDA 040246

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

FDA NDC Directory listings under ANDA 040246
ProductStrengthForm · routeLabelerProduct NDC
ComproprochlorperazineProchlorperazine 25 mg/1SuppositoryRectalPadagis US LLC0574-7226

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