Chlorpromazine Hydrochloride NDC 70518-3674

NDC codes

FDA NDC Directory

Product NDC (as listed)70518-3674Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70518-3674Add 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
70518-3674-0	70518367400	100 POUCH in 1 BOX (70518-3674-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-3674-1)Marketed from Mar 6, 2023
70518-3674-2	70518367402	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3674-2)Marketed from Dec 4, 2023
70518-3674-3	70518367403	100 POUCH in 1 BOX (70518-3674-3) / 1 TABLET, FILM COATED in 1 POUCH (70518-3674-4)Marketed from Aug 14, 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 Hydrochloride
Generic name (nonproprietary): chlorpromazine hydrochloride
Active ingredients: Chlorpromazine hydrochloride — 50 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: REMEDYREPACK INC.
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 084113
Marketing start: Mar 6, 2023
Listing expires: Dec 31, 2027
Other FDA classes: Phenothiazines (Chemical structure)
Identifiers: Product ID 70518-3674_59036347-d875-b4f2-e063-6394a90a3f54SPL ID 59036347-d875-b4f2-e063-6394a90a3f54SPL set ID 41b86f9d-d7e2-4296-8d88-e8257c7cbed2RxCUI 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

N470518367400 followed by a unit qualifier and the quantity

Package 70518-3674-00. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 084113

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

FDA NDC Directory listings under ANDA 084113
Product	Strength	Form · route	Labeler	Product NDC
Chlorpromazine Hydrochloride	Chlorpromazine hydrochloride 50 mg/1	Tablet, Film coatedOral	Upsher-Smith Laboratories, LLC	0832-6019