Prescription drug · ANDA

Fluphenazine Hydrochloride NDC 72205-114

Fluphenazine hydrochloride 5 mg/1 · Tablet, Film coated · Oral · Novadoz Pharmaceuticals LLC

NDC codes

FDA NDC Directory
Product NDC (as listed)72205-114Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72205-0114Add 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
72205-114-0572205011405500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72205-114-05)Marketed from Sep 14, 2023
72205-114-9172205011491100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72205-114-91)Marketed from Sep 14, 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 — 5 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 217189
Marketing start
Listing expires
Other FDA classes
Phenothiazines (Chemical structure)
Identifiers
Product ID 72205-114_f99e9ea5-3c4a-4a94-9ca9-709f65b8fd82SPL ID f99e9ea5-3c4a-4a94-9ca9-709f65b8fd82SPL set ID 83ce71b9-28eb-4074-b1e7-192ed254c529RxCUI 859841, 860918, 865117, 865123UNII ZOU145W1XLUPC 0372205115910, 0372205114913, 0372205112919, 0372205113916, 0372205114050, 0372205112056, 0372205113053
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

N472205011405 followed by a unit qualifier and the quantity

Package 72205-0114-05. 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)

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)

Other NDCs under ANDA 217189

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

FDA NDC Directory listings under ANDA 217189
ProductStrengthForm · routeLabelerProduct NDC
Fluphenazine HydrochlorideFluphenazine hydrochloride 2.5 mg/1Tablet, Film coatedOralNovadoz Pharmaceuticals LLC72205-113
Fluphenazine HydrochlorideFluphenazine hydrochloride 1 mg/1Tablet, Film coatedOralNovadoz Pharmaceuticals LLC72205-112
Fluphenazine HydrochlorideFluphenazine hydrochloride 10 mg/1Tablet, Film coatedOralNovadoz Pharmaceuticals LLC72205-115

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Fluphenazine Hydrochloride NDC 72205-114 | Med-Code