NDC codes

FDA NDC Directory
Product NDC (as listed)71205-979Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71205-0979Add 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
71205-979-0071205097900100 CAPSULE in 1 BOTTLE (71205-979-00)Marketed from May 7, 2020
71205-979-11712050979111000 CAPSULE in 1 BOTTLE (71205-979-11)Marketed from May 7, 2020
71205-979-307120509793030 CAPSULE in 1 BOTTLE (71205-979-30)Marketed from May 7, 2020
71205-979-5571205097955500 CAPSULE in 1 BOTTLE (71205-979-55)Marketed from May 7, 2020
71205-979-607120509796060 CAPSULE in 1 BOTTLE (71205-979-60)Marketed from May 7, 2020
71205-979-7271205097972120 CAPSULE in 1 BOTTLE (71205-979-72)Marketed from May 7, 2020
71205-979-907120509799090 CAPSULE in 1 BOTTLE (71205-979-90)Marketed from May 7, 2020

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 hydrochloride
Active ingredients
Fluoxetine hydrochloride — 40 mg/1
Dosage form
Capsule
Route
Oral
Labeler
Proficient Rx LPNDC labeler code 71205
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 204597
Marketing start
Listing expires
Other FDA classes
Serotonin Uptake Inhibitors (Mechanism)
Identifiers
Product ID 71205-979_14464dfb-94a5-43a1-923e-d462b7ade131SPL ID 14464dfb-94a5-43a1-923e-d462b7ade131SPL set ID 57f21f2b-0ec2-49dc-911a-806e5ae880c2RxCUI 310384, 310385, 313989UNII I9W7N6B1KJUPC 0371205979720, 0371205974305, 0371205975302
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

N471205097900 followed by a unit qualifier and the quantity

Package 71205-0979-00. 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 is 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 and Olanzapine in Combination is indicated for the treatment of: • Acute treatment of depressive episodes associated with Bipolar I Disorder. •…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71205-979

What is NDC 71205-979?
71205-979 is the product NDC for Fluoxetine (fluoxetine hydrochloride), Fluoxetine hydrochloride 40 mg/1 capsule, listed with the FDA by Proficient Rx LP. It has 7 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Fluoxetine (Fluoxetine Hydrochloride).
What is the active ingredient?
Fluoxetine hydrochloride.
Who is the labeler?
Proficient Rx LP, NDC labeler code 71205. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Fluoxetine?
193 other product NDCs are listed under this name. See all Fluoxetine 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 Fluoxetine NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
FluoxetineFluoxetine hydrochloride 40 mg/1CapsuleOralAmerican Health Packaging68002-10568002-0105-01
FluoxetineFluoxetine hydrochloride 20 mg/1CapsuleOralUnit Dose Solutions, Inc.87441-03187441-0031-01
Fluoxetinefluoxetine hydrochlorideFluoxetine hydrochloride 40 mg/1CapsuleOralCoupler LLC67046-055267046-0552-03
Fluoxetinefluoxetine hydrochlorideFluoxetine hydrochloride 10 mg/1CapsuleOralCoupler LLC67046-208367046-2083-03
FluoxetineFluoxetine hydrochloride 10 mg/1CapsuleOralREMEDYREPACK INC.70518-461170518-4611-00
FluoxetineFluoxetine hydrochloride 20 mg/1CapsuleOralCoupler LLC67046-167067046-1670-03
FluoxetineFluoxetine hydrochloride 10 mg/1CapsuleOralNorthwind Health Company, LLC82868-10582868-0105-3082868-0105-90
FluoxetineFluoxetine hydrochloride 20 mg/1CapsuleOralREMEDYREPACK INC.70518-457670518-4576-00
FluoxetineFluoxetine hydrochloride 10 mg/1Tablet, Film coatedOralAurobindo Pharma Limited84386-10484386-0104-0184386-0104-30
FluoxetineFluoxetine hydrochloride 60 mg/1Tablet, Film coatedOralAurobindo Pharma Limited84386-10684386-0106-30

All 194 Fluoxetine NDCs

Other NDCs under ANDA 204597

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

FDA NDC Directory listings under ANDA 204597
ProductStrengthForm · routeLabelerProduct NDC
Fluoxetinefluoxetine hydrochlorideFluoxetine hydrochloride 10 mg/1CapsuleOralCalvin Scott & Co., Inc.17224-171
Fluoxetinefluoxetine hydrochlorideFluoxetine hydrochloride 20 mg/1CapsuleOralCalvin Scott & Co., Inc.17224-174
Fluoxetinefluoxetine hydrochlorideFluoxetine hydrochloride 10 mg/1CapsuleOralVensun Pharmaceuticals, Inc.42543-725
Fluoxetinefluoxetine hydrochlorideFluoxetine hydrochloride 20 mg/1CapsuleOralVensun Pharmaceuticals, Inc.42543-726
Fluoxetinefluoxetine hydrochlorideFluoxetine hydrochloride 40 mg/1CapsuleOralVensun Pharmaceuticals, Inc.42543-727
Fluoxetinefluoxetine hydrochlorideFluoxetine hydrochloride 20 mg/1CapsuleOralMedsource Pharmaceuticals45865-174
Fluoxetinefluoxetine hydrochlorideFluoxetine hydrochloride 40 mg/1CapsuleOralA-S Medication Solutions50090-5678
Fluoxetinefluoxetine hydrochlorideFluoxetine hydrochloride 10 mg/1CapsuleOralA-S Medication Solutions50090-6193
Fluoxetinefluoxetine hydrochlorideFluoxetine hydrochloride 20 mg/1CapsuleOralA-S Medication Solutions50090-6574
Fluoxetinefluoxetine hydrochlorideFluoxetine hydrochloride 10 mg/1CapsuleOralA-S Medication Solutions50090-6702
Fluoxetinefluoxetine hydrochlorideFluoxetine hydrochloride 20 mg/1CapsuleOralA-S Medication Solutions50090-7225
Fluoxetinefluoxetine hydrochlorideFluoxetine hydrochloride 20 mg/1CapsuleOralA-S Medication Solutions50090-7226
Fluoxetinefluoxetine hydrochlorideFluoxetine hydrochloride 40 mg/1CapsuleOralA-S Medication Solutions50090-7899
Fluoxetinefluoxetine hydrochlorideFluoxetine hydrochloride 10 mg/1CapsuleOralScieGen Pharmaceuticals, Inc.50228-113
Fluoxetinefluoxetine hydrochlorideFluoxetine hydrochloride 20 mg/1CapsuleOralScieGen Pharmaceuticals, Inc.50228-114
Fluoxetinefluoxetine hydrochlorideFluoxetine hydrochloride 40 mg/1CapsuleOralScieGen Pharmaceuticals, Inc.50228-115
Fluoxetinefluoxetine hydrochlorideFluoxetine hydrochloride 20 mg/1CapsuleOralNorthwind Health Company, LLC51655-274
Fluoxetinefluoxetine hydrochlorideFluoxetine hydrochloride 10 mg/1CapsuleOralNorthwind Health Company, LLC51655-314
Fluoxetinefluoxetine hydrochlorideFluoxetine hydrochloride 20 mg/1CapsuleOralAphena Pharma Solutions - Tennessee, LLC53401-024
Fluoxetinefluoxetine hydrochlorideFluoxetine hydrochloride 20 mg/1CapsuleOralSt. Mary's Medical Park Pharmacy60760-311

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