What is NDC 37662-0337?

37662-0337 is the product NDC for Citalopram, Citalopram 12 [hp_C]/1 pellet, listed with the FDA by Hahnemann Laboratories, INC.. It has 3 package NDCs, shown above in 10- and 11-digit form.

Hahnemann Laboratories, INC., NDC labeler code 37662. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Citalopram?

92 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Citalopram NDC 37662-0337 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)37662-0337Labeler and product segments. Claims need a package NDC.

Product NDC at billing width37662-0337Add 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
37662-0337-1	37662033701	200 PELLET in 1 VIAL, GLASS (37662-0337-1)Marketed from Jun 6, 2022
37662-0337-2	37662033702	1200 PELLET in 1 BOTTLE, GLASS (37662-0337-2)Marketed from Jun 6, 2022
37662-0337-3	37662033703	4000 PELLET in 1 BOTTLE, GLASS (37662-0337-3)Marketed from Jun 6, 2022

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): Citalopram
Generic name (nonproprietary): citalopram
Active ingredients: Citalopram — 12 [hp_C]/1
Dosage form: Pellet
Route: Oral
Labeler: Hahnemann Laboratories, INC.NDC labeler code 37662
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jun 6, 2022
Listing expires: Dec 31, 2026
Other FDA classes: Serotonin Uptake Inhibitors (Mechanism)
Identifiers: Product ID 37662-0337_e0cc472a-dbac-71c3-e053-2995a90adf50SPL ID e0cc472a-dbac-71c3-e053-2995a90adf50SPL set ID e0cc472a-dbab-71c3-e053-2995a90adf50UNII 0DHU5B8D6V
Pharmacologic class: Serotonin Reuptake Inhibitor

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

N437662033701 followed by a unit qualifier and the quantity

Package 37662-0337-01. 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 6, 2022.

Full label on DailyMed (opens in a new tab)

About NDC 37662-0337

What is NDC 37662-0337?: 37662-0337 is the product NDC for Citalopram, Citalopram 12 [hp_C]/1 pellet, listed with the FDA by Hahnemann Laboratories, INC.. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Citalopram.
What is the active ingredient?: Citalopram.
Who is the labeler?: Hahnemann Laboratories, INC., NDC labeler code 37662. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Citalopram?: 92 other product NDCs are listed under this name. See all Citalopram 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 Citalopram NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Citalopram	Citalopram hydrobromide 40 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-0113	67046-0113-03
Citalopram	Citalopram hydrobromide 10 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-0793	67046-0793-03
Citalopram	Citalopram hydrobromide 20 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-0795	67046-0795-03
Citalopram	Citalopram hydrobromide 30 mg/1	CapsuleOral	Aurobindo Pharma Limited	59651-964	59651-0964-30
Citalopram	Citalopram hydrobromide 10 mg/1	Tablet, Film coatedOral	Advanced Rx of Tennessee, LLC	80425-0557	80425-0557-0180425-0557-0280425-0557-03
Citalopram	Citalopram hydrobromide 10 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4476	70518-4476-0070518-4476-01
Citalopram	Citalopram hydrobromide 10 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4416	70518-4416-00
Citalopram	Citalopram hydrobromide 20 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4335	70518-4335-0070518-4335-0170518-4335-02+1 more
Citalopramcitalopram hydrobromide	Citalopram hydrobromide 40 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4334	70518-4334-0070518-4334-02
Citalopramcitalopram hydrobromide	Citalopram hydrobromide 20 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4114	70518-4114-01

All 93 Citalopram NDCs