What is NDC 31722-367?

31722-367 is the product NDC for Chlorpromazine Hydrochloride, Chlorpromazine hydrochloride 25 mg/mL injection, listed with the FDA by Camber Pharmaceuticals, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

Camber Pharmaceuticals, Inc., NDC labeler code 31722. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Chlorpromazine Hydrochloride?

106 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Chlorpromazine Hydrochloride NDC 31722-367

NDC codes

FDA NDC Directory

Product NDC (as listed)31722-367Labeler and product segments. Claims need a package NDC.

Product NDC at billing width31722-0367Add 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
31722-367-32	3172203673231722036732	25 VIAL in 1 CARTON (31722-367-32) / 2 mL in 1 VIAL (31722-367-31)Marketed from Nov 18, 2024

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): Chlorpromazine Hydrochloride
Generic name (nonproprietary): chlorpromazine hydrochloride
Active ingredients: Chlorpromazine hydrochloride — 25 mg/mL
Dosage form: Injection
Route: Intramuscular
Labeler: Camber Pharmaceuticals, Inc.NDC labeler code 31722
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 218272
Marketing start: Nov 18, 2024
Listing expires: Dec 31, 2026
Other FDA classes: Phenothiazines (Chemical structure)
Identifiers: Product ID 31722-367_2d38c8d4-8ed5-0840-e063-6294a90a904fSPL ID 2d38c8d4-8ed5-0840-e063-6294a90a904fSPL set ID 6564346c-661c-41cf-9cef-db6aa15710cdRxCUI 1730076, 1730078UNII 9WP59609J6UPC 0331722367318
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.

Administration

Drug administration (CPT 96360–96549)

When a clinician administers the drug, the administration is reported separately. Codes in this range cover hydration, therapeutic injections and infusions, and chemotherapy or other complex drug administration. The right code depends on route, duration and drug type, and self-administered drugs are not billed this way.

How CPT relates to drug billing

NDC on a medical claim

N431722036732 followed by a unit qualifier and the quantity

Package 31722-0367-32. 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 Feb 3, 2025. This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE 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 accompanying conduct disorders consisting of some or all of the followi…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 31722-367

What is NDC 31722-367?: 31722-367 is the product NDC for Chlorpromazine Hydrochloride, Chlorpromazine hydrochloride 25 mg/mL injection, listed with the FDA by Camber Pharmaceuticals, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Chlorpromazine Hydrochloride.
What is the active ingredient?: Chlorpromazine hydrochloride.
Who is the labeler?: Camber Pharmaceuticals, Inc., NDC labeler code 31722. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Chlorpromazine Hydrochloride?: 106 other product NDCs are listed under this name. See all Chlorpromazine Hydrochloride 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 Chlorpromazine Hydrochloride NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Chlorpromazine Hydrochloride	Chlorpromazine hydrochloride 25 mg/1	Tablet, Sugar coatedOral	American Health Packaging	60687-938	60687-0938-0160687-0938-65
Chlorpromazine Hydrochloride	Chlorpromazine hydrochloride 50 mg/1	Tablet, Sugar coatedOral	American Health Packaging	60687-949	60687-0949-01
Chlorpromazine Hydrochloride	Chlorpromazine hydrochloride 100 mg/1	Tablet, Sugar coatedOral	American Health Packaging	60687-960	60687-0960-01
Chlorpromazine Hydrochloride	Chlorpromazine hydrochloride 200 mg/1	Tablet, Sugar coatedOral	American Health Packaging	60687-971	60687-0971-01
Chlorpromazine Hydrochloride	Chlorpromazine hydrochloride 100 mg/mL	ConcentrateOral	Saptalis Pharmaceuticals, LLC.	71656-101	71656-0101-08
Chlorpromazine Hydrochloride	Chlorpromazine hydrochloride 30 mg/mL	ConcentrateOral	Saptalis Pharmaceuticals, LLC.	71656-102	71656-0102-04
Chlorpromazine Hydrochloride	Chlorpromazine hydrochloride 25 mg/mL	InjectionIntramuscular	Novadoz Pharmaceuticals LLC	72205-190	72205-0190-25
Chlorpromazine Hydrochloride	Chlorpromazine hydrochloride 25 mg/mL	InjectionIntramuscular	Novadoz Pharmaceuticals LLC	72205-191	72205-0191-25
Chlorpromazine Hydrochloride	Chlorpromazine hydrochloride 25 mg/1	Tablet, Sugar coatedOral	Coupler LLC	67046-1633	67046-1633-03
chlorpromazine hydrochloride	Chlorpromazine hydrochloride 30 mg/mL	ConcentrateOral	Advagen Pharma Ltd	72888-457	72888-0457-01

All 107 Chlorpromazine Hydrochloride NDCs

Other NDCs under ANDA 218272

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

FDA NDC Directory listings under ANDA 218272
Product	Strength	Form · route	Labeler	Product NDC
Chlorpromazine Hydrochloride	Chlorpromazine hydrochloride 25 mg/mL	InjectionIntramuscular	Camber Pharmaceuticals, Inc.	31722-366