What is NDC 60687-971?

60687-971 is the product NDC for Chlorpromazine Hydrochloride, Chlorpromazine hydrochloride 200 mg/1 tablet, sugar coated, listed with the FDA by American Health Packaging. It has 1 package NDC, shown above in 10- and 11-digit form.

American Health Packaging, NDC labeler code 60687. 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 60687-971

NDC codes

FDA NDC Directory

Product NDC (as listed)60687-971Labeler and product segments. Claims need a package NDC.

Product NDC at billing width60687-0971Add 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
60687-971-01	6068709710160687097101	100 BLISTER PACK in 1 CARTON (60687-971-01) / 1 TABLET, SUGAR COATED in 1 BLISTER PACK (60687-971-11)Marketed from May 17, 2026

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 — 200 mg/1
Dosage form: Tablet, Sugar coated
Route: Oral
Labeler: American Health PackagingNDC labeler code 60687
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 214827
Marketing start: May 17, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Phenothiazines (Chemical structure)
Identifiers: Product ID 60687-971_5348eb0c-95eb-da92-e063-6294a90a9a5cSPL ID 5348eb0c-95eb-da92-e063-6294a90a9a5cSPL set ID 85ab0b93-c716-4889-87db-9e76e75df7c7RxCUI 991044, 991188, 991194, 991336UNII 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

N460687097101 followed by a unit qualifier and the quantity

Package 60687-0971-01. 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 Jun 2, 2026. 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)

About NDC 60687-971

What is NDC 60687-971?: 60687-971 is the product NDC for Chlorpromazine Hydrochloride, Chlorpromazine hydrochloride 200 mg/1 tablet, sugar coated, listed with the FDA by American Health Packaging. 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?: American Health Packaging, NDC labeler code 60687. 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 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	72205-191	72205-0191-25
Chlorpromazine Hydrochloride	Chlorpromazine hydrochloride 25 mg/mL	InjectionIntramuscular	Novadoz Pharmaceuticals LLC	72205-190	72205-0190-25
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
chlorpromazine hydrochloride	Chlorpromazine hydrochloride 100 mg/mL	ConcentrateOral	Advagen Pharma Ltd	72888-458	72888-0458-01

All 107 Chlorpromazine Hydrochloride NDCs

Other NDCs under ANDA 214827

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

FDA NDC Directory listings under ANDA 214827
Product	Strength	Form · route	Labeler	Product NDC
Chlorpromazine Hydrochloride	Chlorpromazine hydrochloride 25 mg/1	Tablet, Sugar coatedOral	REMEDYREPACK INC.	70518-3510
Chlorpromazine Hydrochloride	Chlorpromazine hydrochloride 50 mg/1	Tablet, Sugar coatedOral	REMEDYREPACK INC.	70518-3549
Chlorpromazine Hydrochloride	Chlorpromazine hydrochloride 25 mg/1	Tablet, Sugar coatedOral	Coupler LLC	67046-1633
Chlorpromazine Hydrochloride	Chlorpromazine hydrochloride 100 mg/1	Tablet, Sugar coatedOral	REMEDYREPACK INC.	70518-3584
Chlorpromazine Hydrochloride	Chlorpromazine hydrochloride 200 mg/1	Tablet, Sugar coatedOral	REMEDYREPACK INC.	70518-4142
Chlorpromazine Hydrochloride	Chlorpromazine hydrochloride 100 mg/1	Tablet, Sugar coatedOral	Novadoz Pharmaceuticals LLC	72205-106
Chlorpromazine Hydrochloride	Chlorpromazine hydrochloride 25 mg/1	Tablet, Sugar coatedOral	Novadoz Pharmaceuticals LLC	72205-104
Chlorpromazine Hydrochloride	Chlorpromazine hydrochloride 50 mg/1	Tablet, Sugar coatedOral	Novadoz Pharmaceuticals LLC	72205-105
Chlorpromazine Hydrochloride	Chlorpromazine hydrochloride 200 mg/1	Tablet, Sugar coatedOral	Novadoz Pharmaceuticals LLC	72205-107
Chlorpromazine Hydrochloride	Chlorpromazine hydrochloride 25 mg/1	Tablet, Sugar coatedOral	American Health Packaging	60687-938
Chlorpromazine Hydrochloride	Chlorpromazine hydrochloride 50 mg/1	Tablet, Sugar coatedOral	American Health Packaging	60687-949
Chlorpromazine Hydrochloride	Chlorpromazine hydrochloride 100 mg/1	Tablet, Sugar coatedOral	American Health Packaging	60687-960
Chlorpromazine Hydrochloride	Chlorpromazine hydrochloride 50 mg/1	Tablet, Sugar coatedOral	Coupler LLC	67046-1563