NDC codes

FDA NDC Directory
Product NDC (as listed)71335-0238Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-0238Add 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
71335-0238-1713350238017133502380130 TABLET in 1 BOTTLE (71335-0238-1)Marketed from May 18, 2018
71335-0238-2713350238027133502380260 TABLET in 1 BOTTLE (71335-0238-2)Marketed from Sep 19, 2018
71335-0238-3713350238037133502380390 TABLET in 1 BOTTLE (71335-0238-3)Marketed from Apr 17, 2018
71335-0238-47133502380471335023804100 TABLET in 1 BOTTLE (71335-0238-4)Marketed from Jun 24, 2020
71335-0238-5713350238057133502380515 TABLET in 1 BOTTLE (71335-0238-5)Marketed from Oct 30, 2024
71335-0238-67133502380671335023806120 TABLET in 1 BOTTLE (71335-0238-6)Marketed from Sep 5, 2019
71335-0238-771335023807713350238077 TABLET in 1 BOTTLE (71335-0238-7)Marketed from Oct 30, 2024

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 Hydrobromide
Generic name (nonproprietary)
citalopram hydrobromide
Active ingredients
Citalopram hydrobromide — 20 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Bryant Ranch PrepackNDC labeler code 71335
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 71335-0238_e98dc453-0638-4318-9778-e9a881646d36SPL ID e98dc453-0638-4318-9778-e9a881646d36SPL set ID 8719bd44-36b6-468d-9203-8c53a2645184RxCUI 200371UNII 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

N471335023801 followed by a unit qualifier and the quantity

Package 71335-0238-01. 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)

About NDC 71335-0238

What is NDC 71335-0238?
71335-0238 is the product NDC for Citalopram Hydrobromide, Citalopram hydrobromide 20 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 7 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Citalopram Hydrobromide.
What is the active ingredient?
Citalopram hydrobromide.
Who is the labeler?
Bryant Ranch Prepack, NDC labeler code 71335. 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 Hydrobromide?
28 other product NDCs are listed under this name. See all Citalopram Hydrobromide 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 Hydrobromide NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Citalopram HydrobromideCitalopram hydrobromide 10 mg/1Tablet, Film coatedOralAdvanced Rx Pharmacy of Tennessee, LLC80425-030980425-0309-0180425-0309-0280425-0309-03
Citalopram HydrobromideCitalopram hydrobromide 10 mg/1Tablet, Film coatedOralNorthwind Health Company, LLC51655-04351655-0043-2651655-0043-52
Citalopram HydrobromideCitalopram hydrobromide 20 mg/1TabletOralQuality Care Products, LLC55700-85155700-0851-90
Citalopram HydrobromideCitalopram hydrobromide 10 mg/1TabletOralQuality Care Products, LLC55700-78755700-0787-3055700-0787-90
Citalopram HydrobromideCitalopram hydrobromide 10 mg/5mLSolutionOralATLANTIC BIOLOGICALS CORP.17856-056417856-0564-01
Citalopram HydrobromidecitalopramCitalopram hydrobromide 20 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-09271610-0092-1571610-0092-3071610-0092-45+1 more
Citalopram HydrobromidecitalopramCitalopram hydrobromide 10 mg/1TabletOralExelan Pharmaceuticals Inc.76282-62876282-0628-0576282-0628-1076282-0628-30+1 more
Citalopram HydrobromidecitalopramCitalopram hydrobromide 20 mg/1TabletOralExelan Pharmaceuticals Inc.76282-62976282-0629-0576282-0629-1076282-0629-30+1 more
Citalopram HydrobromideCitalopram hydrobromide 40 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals Inc.68788-896268788-8962-0168788-8962-0368788-8962-06+2 more
Citalopram HydrobromideCitalopram hydrobromide 10 mg/5mLSolutionOralCamber Pharmaceuticals, Inc.31722-56431722-0564-24

All 29 Citalopram Hydrobromide NDCs

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
CitalopramCitalopram hydrobromide 10 mg/1Tablet, Film coatedOralCardinal Health 107, LLC55154-3349
CitalopramCitalopram hydrobromide 20 mg/1Tablet, Film coatedOralCardinal Health 107, LLC55154-3329
Citalopram HydrobromideCitalopram hydrobromide 20 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-1830
Citalopram HydrobromideCitalopram hydrobromide 20 mg/1TabletOralProficient Rx LP63187-203
CitalopramCitalopram hydrobromide 40 mg/1Tablet, Film coatedOralCoupler LLC67046-0113
Citalopram HydrobromideCitalopram hydrobromide 20 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-1906
Citalopram HydrobromideCitalopram hydrobromide 10 mg/1TabletOralProficient Rx LP63187-220
CitalopramCitalopram hydrobromide 10 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.43063-481
CitalopramCitalopram hydrobromide 40 mg/1Tablet, Film coatedOralASCLEMED USA INC.87063-221
CitalopramCitalopram hydrobromide 10 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-4476
Citalopram HydrobromideCitalopram hydrobromide 20 mg/1TabletOralNuCare Pharmaceuticals, Inc.68071-2198
Citalopram HydrobromideCitalopram hydrobromide 20 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-5132
Citalopram HydrobromideCitalopram hydrobromide 10 mg/1Tablet, Film coatedOralNorthwind Health Company, LLC51655-043
Citalopram HydrobromideCitalopram hydrobromide 20 mg/1TabletOralA-S Medication Solutions50090-6846
Citalopram HydrobromideCitalopram hydrobromide 20 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals, Inc.68788-0802
CitalopramCitalopram hydrobromide 20 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.43063-683
CitalopramCitalopram hydrobromide 20 mg/1Tablet, Film coatedOralQPharma, Inc.42708-091
CitalopramCitalopram hydrobromide 10 mg/1Tablet, Film coatedOralTorrent Pharmaceuticals Limited13668-009
CitalopramCitalopram hydrobromide 20 mg/1Tablet, Film coatedOralTorrent Pharmaceuticals Limited13668-010
CitalopramCitalopram hydrobromide 40 mg/1Tablet, Film coatedOralTorrent Pharmaceuticals Limited13668-011

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