Prescription drug · ANDA
Citalopram NDC 71335-2232
Citalopram hydrobromide 40 mg/1 · Tablet, Film coated · Oral · Bryant Ranch Prepack
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 71335-2232-1 | 71335223201 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2232-1)Marketed from Sep 18, 2023 | |
| 71335-2232-2 | 71335223202 | 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2232-2)Marketed from Oct 4, 2024 | |
| 71335-2232-3 | 71335223203 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2232-3)Marketed from Oct 4, 2024 | |
| 71335-2232-4 | 71335223204 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2232-4)Marketed from Sep 18, 2023 | |
| 71335-2232-5 | 71335223205 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2232-5)Marketed from Oct 4, 2024 | |
| 71335-2232-6 | 71335223206 | 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2232-6)Marketed from Oct 4, 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
- Generic name (nonproprietary)
- citalopram
- Active ingredients
- Citalopram hydrobromide — 40 mg/1
- Dosage form
- Tablet, Film coated
- Route
- Oral
- Labeler
- Bryant Ranch Prepack
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 077042
- Marketing start
- Listing expires
- Other FDA classes
- Serotonin Uptake Inhibitors (Mechanism)
- Identifiers
- Product ID 71335-2232_ff4ddb77-91cf-4e45-b855-55e4c264d085SPL ID ff4ddb77-91cf-4e45-b855-55e4c264d085SPL set ID 2a8acad8-0ba0-4631-9f6d-f587e7a8558cRxCUI 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
N471335223201followed by a unit qualifier and the quantityPackage 71335-2232-01. 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 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.
Other NDCs under ANDA 077042
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Citalopram | Citalopram hydrobromide 10 mg/1 | Tablet, Film coatedOral | Mylan Pharmaceuticals Inc. | 0378-6231 |
| Citalopram | Citalopram hydrobromide 20 mg/1 | Tablet, Film coatedOral | Mylan Pharmaceuticals Inc. | 0378-6232 |
| Citalopram | Citalopram hydrobromide 40 mg/1 | Tablet, Film coatedOral | Mylan Pharmaceuticals Inc. | 0378-6233 |
| Citalopram | Citalopram hydrobromide 10 mg/1 | Tablet, Film coatedOral | REMEDYREPACK INC. | 70518-2553 |
| Citalopram | Citalopram hydrobromide 40 mg/1 | Tablet, Film coatedOral | REMEDYREPACK INC. | 70518-2601 |
| Citalopram | Citalopram hydrobromide 40 mg/1 | Tablet, Film coatedOral | NuCare Pharmaceuticals,Inc. | 68071-3558 |