What is NDC 71205-838?

71205-838 is the product NDC for Fluphenazine Hydrochloride, Fluphenazine hydrochloride 2.5 mg/1 tablet, film coated, listed with the FDA by Proficient Rx LP. It has 9 package NDCs, shown above in 10- and 11-digit form.

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 Fluphenazine Hydrochloride?

101 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Fluphenazine Hydrochloride NDC 71205-838

NDC codes

FDA NDC Directory

Product NDC (as listed)71205-838Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71205-0838Add 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 NDC	11-digit (billing)	Package
71205-838-00	71205083800	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-838-00)Marketed from Feb 21, 2023
71205-838-11	71205083811	1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-838-11)Marketed from Feb 21, 2023
71205-838-30	71205083830	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-838-30)Marketed from Feb 21, 2023
71205-838-55	71205083855	500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-838-55)Marketed from Feb 21, 2023
71205-838-60	71205083860	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-838-60)Marketed from Feb 21, 2023
71205-838-64	71205083864	240 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-838-64)Marketed from Feb 21, 2023
71205-838-72	71205083872	120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-838-72)Marketed from Feb 21, 2023
71205-838-78	71205083878	180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-838-78)Marketed from Feb 21, 2023
71205-838-90	71205083890	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-838-90)Marketed from Feb 21, 2023

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): Fluphenazine Hydrochloride
Generic name (nonproprietary): fluphenazine hydrochloride
Active ingredients: Fluphenazine hydrochloride — 2.5 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Proficient Rx LPNDC labeler code 71205
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 215848
Marketing start: Aug 1, 2022
Listing expires: Dec 31, 2026
Other FDA classes: Phenothiazines (Chemical structure)
Identifiers: Product ID 71205-838_bc22941e-d2e7-4165-91ea-7239c8b9882dSPL ID bc22941e-d2e7-4165-91ea-7239c8b9882dSPL set ID bc22941e-d2e7-4165-91ea-7239c8b9882dRxCUI 859841, 860918, 865117, 865123UNII ZOU145W1XLUPC 0371205839307, 0371205837303, 0371205838300, 0371205840303
Pharmacologic class: Phenothiazine

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

N471205083800 followed by a unit qualifier and the quantity

Package 71205-0838-00. 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 Feb 1, 2023. This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Fluphenazine hydrochloride tablets are indicated in the management of manifestations of psychotic disorders. Fluphenazine hydrochloride has not been shown effective in the management of behavioral complications in patients with mental retardation.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71205-838

What is NDC 71205-838?: 71205-838 is the product NDC for Fluphenazine Hydrochloride, Fluphenazine hydrochloride 2.5 mg/1 tablet, film coated, listed with the FDA by Proficient Rx LP. It has 9 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Fluphenazine Hydrochloride.
What is the active ingredient?: Fluphenazine 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 Fluphenazine Hydrochloride?: 101 other product NDCs are listed under this name. See all Fluphenazine Hydrochloride 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 Fluphenazine Hydrochloride NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
fluphenazine hydrochloride	Fluphenazine hydrochloride 1 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-0975	67046-0975-03
Fluphenazine Hydrochloride	Fluphenazine hydrochloride 10 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4673	70518-4673-00
Fluphenazine Hydrochloride	Fluphenazine hydrochloride 5 mg/1	Tablet, Film coatedOral	Camber Pharmaceuticals, Inc.	31722-386	31722-0386-0131722-0386-05
Fluphenazine Hydrochloride	Fluphenazine hydrochloride 1 mg/1	Tablet, Film coatedOral	Camber Pharmaceuticals, Inc.	31722-384	31722-0384-0131722-0384-05
Fluphenazine Hydrochloride	Fluphenazine hydrochloride 2.5 mg/1	Tablet, Film coatedOral	Camber Pharmaceuticals, Inc.	31722-385	31722-0385-0131722-0385-05
Fluphenazine Hydrochloride	Fluphenazine hydrochloride 10 mg/1	Tablet, Film coatedOral	Camber Pharmaceuticals, Inc.	31722-387	31722-0387-0131722-0387-05
Fluphenazine Hydrochloride	Fluphenazine hydrochloride 1 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-1567	67046-1567-03
Fluphenazine Hydrochloride	Fluphenazine hydrochloride 5 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-1547	67046-1547-03
Fluphenazine hydrochloride	Fluphenazine hydrochloride 5 mg/1	TabletOral	REMEDYREPACK INC.	70518-4273	70518-4273-0070518-4273-01
Fluphenazine Hydrochloride	Fluphenazine hydrochloride 2.5 mg/1	Tablet, Film coatedOral	Alembic Pharmaceuticals Inc.	62332-789	62332-0789-3162332-0789-71

All 102 Fluphenazine Hydrochloride NDCs

Other NDCs under ANDA 215848

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

FDA NDC Directory listings under ANDA 215848
Product	Strength	Form · route	Labeler	Product NDC
Fluphenazine Hydrochloride	Fluphenazine hydrochloride 5 mg/1	Tablet, Film coatedOral	Proficient Rx LP	71205-839
Fluphenazine Hydrochloride	Fluphenazine hydrochloride 1 mg/1	Tablet, Film coatedOral	Proficient Rx LP	71205-837
Fluphenazine Hydrochloride	Fluphenazine hydrochloride 10 mg/1	Tablet, Film coatedOral	Proficient Rx LP	71205-840
Fluphenazine Hydrochloride	Fluphenazine hydrochloride 1 mg/1	Tablet, Film coatedOral	Upsher-Smith Laboratories, LLC	24979-136
Fluphenazine Hydrochloride	Fluphenazine hydrochloride 2.5 mg/1	Tablet, Film coatedOral	Upsher-Smith Laboratories, LLC	24979-137
Fluphenazine Hydrochloride	Fluphenazine hydrochloride 5 mg/1	Tablet, Film coatedOral	Upsher-Smith Laboratories, LLC	24979-138
Fluphenazine Hydrochloride	Fluphenazine hydrochloride 10 mg/1	Tablet, Film coatedOral	Upsher-Smith Laboratories, LLC	24979-139