NDC codes

FDA NDC Directory
Product NDC (as listed)13668-010Labeler and product segments. Claims need a package NDC.
Product NDC at billing width13668-0010Add 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
13668-010-0113668001001100 TABLET, FILM COATED in 1 BOTTLE (13668-010-01)Marketed from Oct 18, 2007
13668-010-0513668001005500 TABLET, FILM COATED in 1 BOTTLE (13668-010-05)Marketed from Oct 18, 2007
13668-010-06136680010065600 TABLET, FILM COATED in 1 BOTTLE (13668-010-06)Marketed from Oct 18, 2007
13668-010-301366800103030 TABLET, FILM COATED in 1 BOTTLE (13668-010-30)Marketed from Oct 18, 2007

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)
Citalopram
Generic name (nonproprietary)
citalopram
Active ingredients
Citalopram hydrobromide20 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 078216
Marketing start
Listing expires
Other FDA classes
Serotonin Uptake Inhibitors (Mechanism)
Identifiers
Product ID 13668-010_48423caf-4df2-4653-a8ed-b28462757ed3SPL ID 48423caf-4df2-4653-a8ed-b28462757ed3SPL set ID 04766f1d-7a69-49ed-8fd3-1a6305505d47RxCUI 200371, 283672, 309314UNII I1E9D14F36UPC 0313668010015, 0313668011012
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

N413668001001 followed by a unit qualifier and the quantity

Package 13668-0010-01. 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 . 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 is 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)

Other NDCs under ANDA 078216

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

FDA NDC Directory listings under ANDA 078216
ProductStrengthForm · routeLabelerProduct NDC
Citalopram HydrobromideCitalopram hydrobromide 10 mg/1TabletOralProficient Rx LP63187-220
Citalopram HydrobromideCitalopram hydrobromide 20 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-1906
CitalopramCitalopram hydrobromide 40 mg/1Tablet, Film coatedOralCoupler LLC67046-0113
CitalopramCitalopram hydrobromide 10 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-4476
Citalopram HydrobromideCitalopram hydrobromide 40 mg/1TabletOralA-S Medication Solutions50090-3208
Citalopram HydrobromideCitalopram hydrobromide 10 mg/1Tablet, Film coatedOralNorthwind Health Company, LLC51655-043
Citalopram HydrobromideCitalopram hydrobromide 20 mg/1TabletOralNuCare Pharmaceuticals, Inc.68071-2198
Citalopram HydrobromideCitalopram hydrobromide 20 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-5132
CitalopramCitalopram hydrobromide 10 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-0377
Citalopram HydrobromideCitalopram hydrobromide 20 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals, Inc.68788-0802
Citalopram HydrobromideCitalopram hydrobromide 40 mg/1TabletOralBryant Ranch Prepack71335-0480
CitalopramCitalopram hydrobromide 40 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.72789-071
Citalopram HydrobromideCitalopram hydrobromide 40 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-3384
CitalopramCitalopram hydrobromide 10 mg/1Tablet, Film coatedOralMajor Pharmaceuticals0904-6084
CitalopramCitalopram hydrobromide 20 mg/1Tablet, Film coatedOralNorthwind Health Company, LLC51655-664
CitalopramCitalopram hydrobromide 40 mg/1Tablet, Film coatedOralNorthwind Health Company, LLC51655-667
Citalopram HydrobromideCitalopram hydrobromide 20 mg/1TabletOralA-S Medication Solutions50090-6846
CitalopramCitalopram hydrobromide 20 mg/1Tablet, Film coatedOralMajor Pharmaceuticals0904-6085
CitalopramCitalopram hydrobromide 20 mg/1Tablet, Film coatedOralBryant Ranch Prepack72162-2567
CitalopramCitalopram hydrobromide 10 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.43063-481

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