Prescription drug · ANDA
Fluoxetine NDC 72241-007
Fluoxetine hydrochloride 10 mg/1 · Capsule · Oral · Modavar Pharmaceuticals LLC
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 72241-007-05 | 72241000705 | 100 CAPSULE in 1 BOTTLE (72241-007-05)Marketed from Sep 8, 2021 | |
| 72241-007-10 | 72241000710 | 500 CAPSULE in 1 BOTTLE (72241-007-10)Marketed from Sep 8, 2021 | |
| 72241-007-11 | 72241000711 | 1000 CAPSULE in 1 BOTTLE (72241-007-11)Marketed from Sep 8, 2021 | |
| 72241-007-22 | 72241000722 | 30 CAPSULE in 1 BOTTLE (72241-007-22)Marketed from Sep 8, 2021 |
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)
- Fluoxetine
- Generic name (nonproprietary)
- fluoxetine
- Active ingredients
- Fluoxetine hydrochloride — 10 mg/1
- Dosage form
- Capsule
- Route
- Oral
- Labeler
- Modavar Pharmaceuticals LLC
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 206993
- Marketing start
- Listing expires
- Other FDA classes
- Serotonin Uptake Inhibitors (Mechanism)
- Identifiers
- Product ID 72241-007_f35d566f-6a36-4ba8-8f78-6c1d79900e9aSPL ID f35d566f-6a36-4ba8-8f78-6c1d79900e9aSPL set ID 05b0781b-50e2-4311-bde0-430b96e2ef8eRxCUI 310384, 310385, 313989UNII I9W7N6B1KJUPC 0372241008115, 0372241007224, 0372241008221, 0372241009228
- 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
N472241000705followed by a unit qualifier and the quantityPackage 72241-0007-05. 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)
Fluoxetine capsules are indicated for the treatment of: • Acute and maintenance treatment of Major Depressive Disorder [ see Clinical Studies (14.1)]. • Acute and maintenance treatment of obsessions and compulsions in patients with Obsessive Compulsive Disorder (OCD) [ see Clinical Studies (14.2 )]. • Acute and maintenance treatment of binge-eating and vomiting behaviors in patients with moderate to severe Bulimia Nervosa [ see Clinical Studies (14.3 )]. • Acute treatment of Panic Disorder, with or without agoraphobia [ see Clinical Studies (14.4 ) ]. Fluoxetine capsules and Olanzapine in Combination is indicated for the treatment of: • Acute treatment of depressive episodes associated with …
Excerpt only. Read the full label for complete information.
Other NDCs under ANDA 206993
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 |
|---|---|---|---|---|
| Fluoxetine | Fluoxetine hydrochloride 20 mg/1 | CapsuleOral | Coupler LLC | 67046-1670 |
| Fluoxetine | Fluoxetine hydrochloride 10 mg/1 | CapsuleOral | PD-Rx Pharmaceuticals, Inc. | 72789-557 |
| Fluoxetine | Fluoxetine hydrochloride 20 mg/1 | CapsuleOral | Modavar Pharmaceuticals LLC | 72241-008 |
| Fluoxetine | Fluoxetine hydrochloride 40 mg/1 | CapsuleOral | Modavar Pharmaceuticals LLC | 72241-009 |
| Fluoxetine | Fluoxetine hydrochloride 20 mg/1 | CapsuleOral | Cadila Pharmaceuticals Limited | 71209-041 |
| Fluoxetine | Fluoxetine hydrochloride 10 mg/1 | CapsuleOral | Cadila Pharmaceuticals Limited | 71209-040 |
| Fluoxetine | Fluoxetine hydrochloride 40 mg/1 | CapsuleOral | Cadila Pharmaceuticals Limited | 71209-042 |