What is NDC 0832-0111?

0832-0111 is the product NDC for Amantadine Hydrochloride, Amantadine hydrochloride 100 mg/1 tablet, listed with the FDA by Upsher-Smith Laboratories, LLC. It has 2 package NDCs, shown above in 10- and 11-digit form.

Upsher-Smith Laboratories, LLC, NDC labeler code 0832. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Amantadine Hydrochloride?

40 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Amantadine Hydrochloride NDC 0832-0111

NDC codes

FDA NDC Directory

Product NDC (as listed)0832-0111Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00832-0111Add 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	Copy
0832-0111-00	00832011100	100 TABLET in 1 BOTTLE (0832-0111-00)Marketed from Dec 15, 2011
0832-0111-50	00832011150	500 TABLET in 1 BOTTLE (0832-0111-50)Marketed from Dec 15, 2011

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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): Amantadine Hydrochloride
Generic name (nonproprietary): amantadine hydrochloride
Active ingredients: Amantadine hydrochloride — 100 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Upsher-Smith Laboratories, LLCNDC labeler code 0832
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 076186
Marketing start: Dec 15, 2011
Marketing end: Feb 29, 2028
Other FDA classes: M2 Protein Inhibitors (Mechanism)
Identifiers: Product ID 0832-0111_45af44df-1a9b-32b6-e063-6394a90acdafSPL ID 45af44df-1a9b-32b6-e063-6394a90acdafSPL set ID 63d9d4aa-5f92-45b0-98d0-d6ec38b727cbRxCUI 849395UNII M6Q1EO9TD0
Pharmacologic class: Influenza A M2 Protein 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

N400832011100 followed by a unit qualifier and the quantity

Package 00832-0111-00. 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 Dec 11, 2025.

Indications (excerpt from the label)

INDICATIONS AND USAGE Amantadine hydrochloride tablets are indicated for the prophylaxis and treatment of signs and symptoms of infection caused by various strains of influenza A virus. Amantadine hydrochloride tablets are also indicated in the treatment of parkinsonism and drug-induced extrapyramidal reactions. Influenza A Prophylaxis Amantadine hydrochloride tablets are indicated for chemoprophylaxis against signs and symptoms of influenza A virus infection. Because amantadine hydrochloride tablets do not completely prevent the host immune response to influenza A infection, individuals who take this drug may still develop immune responses to natural disease or vaccination and may be protec…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 0832-0111

What is NDC 0832-0111?: 0832-0111 is the product NDC for Amantadine Hydrochloride, Amantadine hydrochloride 100 mg/1 tablet, listed with the FDA by Upsher-Smith Laboratories, LLC. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Amantadine Hydrochloride.
What is the active ingredient?: Amantadine hydrochloride.
Who is the labeler?: Upsher-Smith Laboratories, LLC, NDC labeler code 0832. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Amantadine Hydrochloride?: 40 other product NDCs are listed under this name. See all Amantadine 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 Amantadine Hydrochloride NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
amantadine hydrochloride	Amantadine hydrochloride 100 mg/1	CapsuleOral	AvKARE	73190-094	73190-0094-50
Amantadine Hydrochloride	Amantadine hydrochloride 50 mg/5mL	SolutionOral	BAJAJ MEDICAL, LLC	61037-484	61037-0484-03
Amantadine Hydrochloride	Amantadine hydrochloride 100 mg/1	TabletOral	Coupler LLC	67046-1452	67046-1452-03
amantadine hydrochloride	Amantadine hydrochloride 100 mg/1	CapsuleOral	Coupler LLC	67046-1508	67046-1508-03
Amantadine Hydrochloride	Amantadine hydrochloride 100 mg/1	TabletOral	Zhejiang Jutai Pharmaceutical Co., Ltd.	71765-009	71765-0009-01
Amantadine Hydrochloride	Amantadine hydrochloride 50 mg/5mL	SolutionOral	American Health Packaging	60687-797	60687-0797-56
Amantadine Hydrochloride	Amantadine hydrochloride 50 mg/5mL	SolutionOral	Patrin Pharma, Inc.	39328-530	39328-0530-1639328-0530-99
Amantadine Hydrochloride	Amantadine hydrochloride 100 mg/1	Capsule, Liquid filledOral	Strides Pharma Science Limited	64380-862	64380-0862-0664380-0862-07
Amantadine Hydrochloride	Amantadine hydrochloride 100 mg/1	CapsuleOral	Rising Pharma Holdings, Inc.	16571-834	16571-0834-0116571-0834-50
amantadine hydrochloride	Amantadine hydrochloride 100 mg/1	CapsuleOral	EPIC PHARMA LLC	42806-716	42806-0716-0542806-0716-11

All 41 Amantadine Hydrochloride NDCs