Prescription drug · ANDA

Citalopram (Citalopram hydrobromide) NDC 70518-4334

Citalopram hydrobromide 40 mg/1 · Tablet, Film coated · Oral · REMEDYREPACK INC.

NDC codes

FDA NDC Directory
Product NDC (as listed)70518-4334Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70518-4334Add 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 NDC11-digit (billing)PackageCopy
70518-4334-07051843340070518433400100 POUCH in 1 BOX (70518-4334-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-4334-1)Marketed from Apr 28, 2025
70518-4334-2705184334027051843340230 TABLET, FILM COATED in 1 BLISTER PACK (70518-4334-2)Marketed from Aug 25, 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)
Citalopram
Generic name (nonproprietary)
citalopram hydrobromide
Active ingredients
Citalopram hydrobromide — 40 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
REMEDYREPACK INC.NDC labeler code 70518
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 077031
Marketing start
Listing expires
Other FDA classes
Serotonin Uptake Inhibitors (Mechanism)
Identifiers
Product ID 70518-4334_5aacc6ac-f606-7dbf-e063-6394a90ad7ceSPL ID 5aacc6ac-f606-7dbf-e063-6394a90ad7ceSPL set ID 0109f365-bebd-4810-a56f-4451e10245dbRxCUI 309314UNII I1E9D14F36
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

N470518433400 followed by a unit qualifier and the quantity

Package 70518-4334-00. 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

Current FDA label (SPL), effective . This label includes a boxed warning.

Indications (excerpt from the label)

Citalopram tablets are indicated for the treatment of major depressive disorder (MDD) in adults [see Clinical Studies (14) ] . Citalopram tablets are a selective serotonin reuptake inhibitor (SSRI) indicated for the treatment of major depressive disorder (MDD) in adults ( 1 ) .

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 70518-4334

What is NDC 70518-4334?
70518-4334 is the product NDC for Citalopram (citalopram hydrobromide), Citalopram hydrobromide 40 mg/1 tablet, film coated, listed with the FDA by REMEDYREPACK INC.. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Citalopram (Citalopram Hydrobromide).
What is the active ingredient?
Citalopram hydrobromide.
Who is the labeler?
REMEDYREPACK INC., NDC labeler code 70518. 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?
91 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
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
CitalopramCitalopram hydrobromide 40 mg/1Tablet, Film coatedOralCoupler LLC67046-011367046-0113-03
CitalopramCitalopram hydrobromide 10 mg/1Tablet, Film coatedOralCoupler LLC67046-079367046-0793-03
CitalopramCitalopram hydrobromide 20 mg/1Tablet, Film coatedOralCoupler LLC67046-079567046-0795-03
CitalopramCitalopram hydrobromide 30 mg/1CapsuleOralAurobindo Pharma Limited59651-96459651-0964-30
CitalopramCitalopram hydrobromide 10 mg/1Tablet, Film coatedOralAdvanced Rx of Tennessee, LLC80425-055780425-0557-0180425-0557-0280425-0557-03
CitalopramCitalopram hydrobromide 10 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-447670518-4476-0070518-4476-01
CitalopramCitalopram hydrobromide 10 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-441670518-4416-00
CitalopramCitalopram hydrobromide 20 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-433570518-4335-0070518-4335-0170518-4335-02+1 more
Citalopramcitalopram hydrobromideCitalopram hydrobromide 20 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-411470518-4114-01
Citalopramcitalopram hydrobromideCitalopram hydrobromide 10 mg/1Tablet, Film coatedOralQUALLENT PHARMACEUTICALS HEALTH LLC82009-10682009-0106-05

All 92 Citalopram NDCs

Other NDCs under ANDA 077031

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

FDA NDC Directory listings under ANDA 077031
ProductStrengthForm · routeLabelerProduct NDC
Citalopramcitalopram hydrobromideCitalopram hydrobromide 10 mg/1Tablet, Film coatedOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8022
Citalopramcitalopram hydrobromideCitalopram hydrobromide 20 mg/1Tablet, Film coatedOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8023
Citalopramcitalopram hydrobromideCitalopram hydrobromide 40 mg/1Tablet, Film coatedOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8141
Citalopramcitalopram hydrobromideCitalopram hydrobromide 20 mg/1Tablet, Film coatedOralQPharma, Inc.42708-019
Citalopramcitalopram hydrobromideCitalopram hydrobromide 40 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.43063-670
Citalopramcitalopram hydrobromideCitalopram hydrobromide 40 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-3136
Citalopramcitalopram hydrobromideCitalopram hydrobromide 20 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-6433
Citalopramcitalopram hydrobromideCitalopram hydrobromide 40 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-7039
Citalopramcitalopram hydrobromideCitalopram hydrobromide 10 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-7419
Citalopramcitalopram hydrobromideCitalopram hydrobromide 10 mg/1Tablet, Film coatedOralNorthwind Health Company, LLC51655-605
Citalopramcitalopram hydrobromideCitalopram hydrobromide 20 mg/1Tablet, Film coatedOralNorthwind Health Company, LLC51655-680
Citalopramcitalopram hydrobromideCitalopram hydrobromide 40 mg/1Tablet, Film coatedOralProficient Rx LP63187-140
Citalopramcitalopram hydrobromideCitalopram hydrobromide 20 mg/1Tablet, Film coatedOralProficient Rx LP63187-679
Citalopramcitalopram hydrobromideCitalopram hydrobromide 20 mg/1Tablet, Film coatedOralAurobindo Pharma Limited65862-006
Citalopramcitalopram hydrobromideCitalopram hydrobromide 40 mg/1Tablet, Film coatedOralAurobindo Pharma Limited65862-007
Citalopramcitalopram hydrobromideCitalopram hydrobromide 40 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals,Inc.68071-3357
Citalopramcitalopram hydrobromideCitalopram hydrobromide 20 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-4114
Citalopramcitalopram hydrobromideCitalopram hydrobromide 40 mg/1Tablet, Film coatedOralAphena Pharma Solutions - Tennessee, LLC71610-413
Citalopramcitalopram hydrobromideCitalopram hydrobromide 20 mg/1Tablet, Film coatedOralBryant Ranch Prepack72162-2517
Citalopramcitalopram hydrobromideCitalopram hydrobromide 10 mg/1Tablet, Film coatedOralQUALLENT PHARMACEUTICALS HEALTH LLC82009-106

Showing 20 of 23.

Med-Code uses cookies for analytics and advertising. You can accept or reject them; the site works either way. Privacy Policy.

Free account

Log in to keep searching

You’ve used your 3 free searches. Med-Code is free: log in or create a free profile to keep looking up NDCs, J-codes and drugs.

Create a free profileLog in