Prescription drug · ANDA
Citalopram NDC 87063-221
Citalopram hydrobromide 40 mg/1 · Tablet, Film coated · Oral · ASCLEMED USA INC.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 87063-221-01 | 87063022101 | 100 TABLET, FILM COATED in 1 BOTTLE (87063-221-01)Marketed from May 29, 2026 | |
| 87063-221-10 | 87063022110 | 10 TABLET, FILM COATED in 1 BOTTLE (87063-221-10)Marketed from May 29, 2026 | |
| 87063-221-20 | 87063022120 | 20 TABLET, FILM COATED in 1 BOTTLE (87063-221-20)Marketed from May 29, 2026 | |
| 87063-221-30 | 87063022130 | 30 TABLET, FILM COATED in 1 BOTTLE (87063-221-30)Marketed from May 29, 2026 | |
| 87063-221-60 | 87063022160 | 60 TABLET, FILM COATED in 1 BOTTLE (87063-221-60)Marketed from May 29, 2026 | |
| 87063-221-90 | 87063022190 | 90 TABLET, FILM COATED in 1 BOTTLE (87063-221-90)Marketed from May 29, 2026 |
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 hydrobromide — 40 mg/1
- Dosage form
- Tablet, Film coated
- Route
- Oral
- Labeler
- ASCLEMED USA INC.
- 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 87063-221_52ee1af5-9a84-797c-e063-6294a90ab63dSPL ID 52ee1af5-9a84-797c-e063-6294a90ab63dSPL set ID df8db06a-ced7-4dd6-83bd-c61d2f68f1b1RxCUI 200371, 283672, 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
N487063022101followed by a unit qualifier and the quantityPackage 87063-0221-01. 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.
Other NDCs under ANDA 078216
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 Hydrobromide | Citalopram hydrobromide 10 mg/1 | TabletOral | Proficient Rx LP | 63187-220 |
| Citalopram Hydrobromide | Citalopram hydrobromide 20 mg/1 | TabletOral | NuCare Pharmaceuticals,Inc. | 68071-1906 |
| Citalopram | Citalopram hydrobromide 40 mg/1 | Tablet, Film coatedOral | Coupler LLC | 67046-0113 |
| Citalopram | Citalopram hydrobromide 10 mg/1 | Tablet, Film coatedOral | REMEDYREPACK INC. | 70518-4476 |
| Citalopram Hydrobromide | Citalopram hydrobromide 40 mg/1 | TabletOral | A-S Medication Solutions | 50090-3208 |
| Citalopram Hydrobromide | Citalopram hydrobromide 10 mg/1 | Tablet, Film coatedOral | Northwind Health Company, LLC | 51655-043 |
| Citalopram Hydrobromide | Citalopram hydrobromide 20 mg/1 | TabletOral | NuCare Pharmaceuticals, Inc. | 68071-2198 |
| Citalopram Hydrobromide | Citalopram hydrobromide 20 mg/1 | TabletOral | NuCare Pharmaceuticals,Inc. | 68071-5132 |
| Citalopram | Citalopram hydrobromide 10 mg/1 | Tablet, Film coatedOral | Bryant Ranch Prepack | 71335-0377 |
| Citalopram Hydrobromide | Citalopram hydrobromide 20 mg/1 | Tablet, Film coatedOral | Preferred Pharmaceuticals, Inc. | 68788-0802 |
| Citalopram Hydrobromide | Citalopram hydrobromide 40 mg/1 | TabletOral | Bryant Ranch Prepack | 71335-0480 |
| Citalopram | Citalopram hydrobromide 40 mg/1 | Tablet, Film coatedOral | PD-Rx Pharmaceuticals, Inc. | 72789-071 |
| Citalopram Hydrobromide | Citalopram hydrobromide 40 mg/1 | TabletOral | NuCare Pharmaceuticals,Inc. | 68071-3384 |
| Citalopram | Citalopram hydrobromide 10 mg/1 | Tablet, Film coatedOral | Major Pharmaceuticals | 0904-6084 |
| Citalopram | Citalopram hydrobromide 20 mg/1 | Tablet, Film coatedOral | Northwind Health Company, LLC | 51655-664 |
| Citalopram | Citalopram hydrobromide 40 mg/1 | Tablet, Film coatedOral | Northwind Health Company, LLC | 51655-667 |
| Citalopram Hydrobromide | Citalopram hydrobromide 20 mg/1 | TabletOral | A-S Medication Solutions | 50090-6846 |
| Citalopram | Citalopram hydrobromide 20 mg/1 | Tablet, Film coatedOral | Major Pharmaceuticals | 0904-6085 |
| Citalopram | Citalopram hydrobromide 20 mg/1 | Tablet, Film coatedOral | Bryant Ranch Prepack | 72162-2567 |
| Citalopram | Citalopram hydrobromide 10 mg/1 | Tablet, Film coatedOral | PD-Rx Pharmaceuticals, Inc. | 43063-481 |
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