NDC codes

FDA NDC Directory
Product NDC (as listed)70518-4724Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70518-4724Add 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
70518-4724-070518472400100 POUCH in 1 BOX (70518-4724-0) / 1 TABLET in 1 POUCH (70518-4724-1)Marketed from Aug 11, 2026

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)
Chlorpromazine
Generic name (nonproprietary)
chlorpromazine
Active ingredients
Chlorpromazine hydrochloride — 100 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 217350
Marketing start
Listing expires
Other FDA classes
Phenothiazines (Chemical structure)
Identifiers
Product ID 70518-4724_5967410b-42bc-7c9f-e063-6394a90a91ebSPL ID 5967410b-42bc-7c9f-e063-6394a90a91ebSPL set ID 0dc38655-01b1-413e-9139-2466014cb4d0RxCUI 991044UNII 9WP59609J6
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 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

N470518472400 followed by a unit qualifier and the quantity

Package 70518-4724-00. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE For the management of manifestations of psychotic disorders. For the treatment of schizophrenia. To control nausea and vomiting. For relief of restlessness and apprehension before surgery. For acute intermittent porphyria. As an adjunct in the treatment of tetanus. To control the manifestations of the manic type of manic-depressive illness. For relief of intractable hiccups. For the treatment of severe behavioral problems in children (1 to 12 years of age) marked by combativeness and/or explosive hyperexcitable behavior (out of proportion to immediate provocations), and in the short-term treatment of hyperactive children who show excessive motor activity with accompanyi…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 217350

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

FDA NDC Directory listings under ANDA 217350
ProductStrengthForm · routeLabelerProduct NDC
ChlorpromazineChlorpromazine hydrochloride 50 mg/1TabletOralAlembic Pharmaceuticals Inc.62332-737
ChlorpromazineChlorpromazine hydrochloride 10 mg/1TabletOralAlembic Pharmaceuticals Inc.62332-735
ChlorpromazineChlorpromazine hydrochloride 25 mg/1TabletOralAlembic Pharmaceuticals Inc.62332-736
ChlorpromazineChlorpromazine hydrochloride 100 mg/1TabletOralAlembic Pharmaceuticals Inc.62332-738
ChlorpromazineChlorpromazine hydrochloride 200 mg/1TabletOralAlembic Pharmaceuticals Inc.62332-739
ChlorpromazineChlorpromazine hydrochloride 50 mg/1TabletOralAlembic Pharmaceuticals Limited46708-737
ChlorpromazineChlorpromazine hydrochloride 10 mg/1TabletOralAlembic Pharmaceuticals Limited46708-735
ChlorpromazineChlorpromazine hydrochloride 25 mg/1TabletOralAlembic Pharmaceuticals Limited46708-736
ChlorpromazineChlorpromazine hydrochloride 100 mg/1TabletOralAlembic Pharmaceuticals Limited46708-738
ChlorpromazineChlorpromazine hydrochloride 200 mg/1TabletOralAlembic Pharmaceuticals Limited46708-739

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