What is NDC 46708-735?

46708-735 is the product NDC for Chlorpromazine, Chlorpromazine hydrochloride 10 mg/1 tablet, listed with the FDA by Alembic Pharmaceuticals Limited. It has 3 package NDCs, shown above in 10- and 11-digit form.

Alembic Pharmaceuticals Limited, NDC labeler code 46708. 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?

10 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Chlorpromazine NDC 46708-735 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)46708-735Labeler and product segments. Claims need a package NDC.

Product NDC at billing width46708-0735Add 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
46708-735-10	4670807351046708073510	100 BLISTER PACK in 1 CARTON (46708-735-10) / 10 TABLET in 1 BLISTER PACKMarketed from Jul 20, 2023
46708-735-31	4670807353146708073531	100 TABLET in 1 BOTTLE (46708-735-31)Marketed from Jul 20, 2023
46708-735-91	4670807359146708073591	1000 TABLET in 1 BOTTLE (46708-735-91)Marketed from Jul 20, 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): Chlorpromazine
Generic name (nonproprietary): chlorpromazine
Active ingredients: Chlorpromazine hydrochloride — 10 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Alembic Pharmaceuticals LimitedNDC labeler code 46708
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 217350
Marketing start: Jul 20, 2023
Listing expires: Dec 31, 2027
Other FDA classes: Phenothiazines (Chemical structure)
Identifiers: Product ID 46708-735_1f9751ff-33da-44be-9c1f-9bbf88ac543bSPL ID 1f9751ff-33da-44be-9c1f-9bbf88ac543bSPL set ID 1f9751ff-33da-44be-9c1f-9bbf88ac543bRxCUI 991039, 991044, 991188, 991194, 991336UNII 9WP59609J6UPC 0346708736316, 0346708737313, 0346708735319, 0346708738310
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

N446708073510 followed by a unit qualifier and the quantity

Package 46708-0735-10. 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 Jul 24, 2023. 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 46708-735

What is NDC 46708-735?: 46708-735 is the product NDC for Chlorpromazine, Chlorpromazine hydrochloride 10 mg/1 tablet, listed with the FDA by Alembic Pharmaceuticals Limited. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Chlorpromazine.
What is the active ingredient?: Chlorpromazine hydrochloride.
Who is the labeler?: Alembic Pharmaceuticals Limited, NDC labeler code 46708. 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?: 10 other product NDCs are listed under this name. See all Chlorpromazine 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 NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Chlorpromazine	Chlorpromazine hydrochloride 100 mg/1	TabletOral	REMEDYREPACK INC.	70518-4724	70518-4724-00
Chlorpromazine	Chlorpromazine hydrochloride 25 mg/1	TabletOral	Alembic Pharmaceuticals Limited	46708-736	46708-0736-1046708-0736-3146708-0736-91
Chlorpromazine	Chlorpromazine hydrochloride 50 mg/1	TabletOral	Alembic Pharmaceuticals Limited	46708-737	46708-0737-1046708-0737-3146708-0737-91
Chlorpromazine	Chlorpromazine hydrochloride 100 mg/1	TabletOral	Alembic Pharmaceuticals Limited	46708-738	46708-0738-1046708-0738-3146708-0738-91
Chlorpromazine	Chlorpromazine hydrochloride 200 mg/1	TabletOral	Alembic Pharmaceuticals Limited	46708-739	46708-0739-1046708-0739-3146708-0739-91
Chlorpromazine	Chlorpromazine hydrochloride 10 mg/1	TabletOral	Alembic Pharmaceuticals Inc.	62332-735	62332-0735-1062332-0735-3162332-0735-91
Chlorpromazine	Chlorpromazine hydrochloride 25 mg/1	TabletOral	Alembic Pharmaceuticals Inc.	62332-736	62332-0736-1062332-0736-3162332-0736-91
Chlorpromazine	Chlorpromazine hydrochloride 50 mg/1	TabletOral	Alembic Pharmaceuticals Inc.	62332-737	62332-0737-1062332-0737-3162332-0737-91
Chlorpromazine	Chlorpromazine hydrochloride 100 mg/1	TabletOral	Alembic Pharmaceuticals Inc.	62332-738	62332-0738-1062332-0738-3162332-0738-91
Chlorpromazine	Chlorpromazine hydrochloride 200 mg/1	TabletOral	Alembic Pharmaceuticals Inc.	62332-739	62332-0739-1062332-0739-3162332-0739-91

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
Product	Strength	Form · route	Labeler	Product NDC
Chlorpromazine	Chlorpromazine hydrochloride 100 mg/1	TabletOral	REMEDYREPACK INC.	70518-4724
Chlorpromazine	Chlorpromazine hydrochloride 50 mg/1	TabletOral	Alembic Pharmaceuticals Limited	46708-737
Chlorpromazine	Chlorpromazine hydrochloride 25 mg/1	TabletOral	Alembic Pharmaceuticals Limited	46708-736
Chlorpromazine	Chlorpromazine hydrochloride 100 mg/1	TabletOral	Alembic Pharmaceuticals Limited	46708-738
Chlorpromazine	Chlorpromazine hydrochloride 200 mg/1	TabletOral	Alembic Pharmaceuticals Limited	46708-739
Chlorpromazine	Chlorpromazine hydrochloride 50 mg/1	TabletOral	Alembic Pharmaceuticals Inc.	62332-737
Chlorpromazine	Chlorpromazine hydrochloride 10 mg/1	TabletOral	Alembic Pharmaceuticals Inc.	62332-735
Chlorpromazine	Chlorpromazine hydrochloride 25 mg/1	TabletOral	Alembic Pharmaceuticals Inc.	62332-736
Chlorpromazine	Chlorpromazine hydrochloride 100 mg/1	TabletOral	Alembic Pharmaceuticals Inc.	62332-738
Chlorpromazine	Chlorpromazine hydrochloride 200 mg/1	TabletOral	Alembic Pharmaceuticals Inc.	62332-739