AMPHMEDIUM SIGNALFINANCIAL10-K

AMPH shows mixed operational performance with strong balance sheet growth but declining profitability due to a dramatic 1,371% spike in interest expense.

The company successfully launched three new FDA-approved products in 2025-2026, demonstrating strong pipeline execution and regulatory momentum. However, the massive increase in interest expense suggests significant new debt financing that is materially impacting profitability despite continued business growth.

Comparing 2026-02-26 vs 2025-03-03View on EDGAR →
FINANCIAL ANALYSIS

AMPH's balance sheet strengthened with current assets growing 19% and cash increasing 12%, while inventory buildup of 15% supports new product launches. However, profitability deteriorated significantly with net income falling 39% and operating income down 32%, driven primarily by interest expense spiking from $1.8M to $27.2M. The combination of reduced operating cash flow (-27%) and continued share buybacks suggests the company is managing through a period of heavy debt-financed growth investments.

FINANCIAL STATEMENT CHANGES
Interest Expense
P&L
+1371.2%
$1.8M$27.2M

Interest expense surged 1371.2% — significant debt increase or rising rates materially impacting earnings.

Net Income
P&L
-38.5%
$159.5M$98.1M

Net income declined 38.5% — review whether driven by operations, interest costs, or non-recurring items.

Operating Income
P&L
-31.7%
$205.4M$140.4M

Operating income deteriorated sharply — investigate whether driven by one-time charges or structural cost issues.

Operating Cash Flow
Cash Flow
-26.8%
$213.4M$156.1M

Operating cash flow softened — monitor whether temporary working capital timing or structural deterioration.

Current Assets
Balance Sheet
+19.1%
$534.1M$636.0M

Current assets grew 19.1% — improving short-term liquidity or inventory/receivables build.

R&D Expense
P&L
+16.1%
$73.9M$85.8M

R&D investment increased 16.1% — signals commitment to future product development, though near-term margin impact.

Inventory
Balance Sheet
+15.1%
$153.7M$176.9M

Inventory built 15.1% — monitor whether demand supports this build or if write-downs may follow.

Cash & Equivalents
Balance Sheet
+12.2%
$151.6M$170.2M

Cash grew 12.2% — improving liquidity position supports investment and shareholder returns.

Share Buybacks
Cash Flow
-11.6%
$85.5M$75.6M

Buyback activity reduced 11.6% — capital being redeployed elsewhere or cash conservation underway.

Stockholders Equity
Balance Sheet
+10.7%
$402.3M$445.5M

Equity base grew 10.7% — retained earnings accumulation or equity issuance strengthening the balance sheet.

LANGUAGE CHANGES
NEW — 2026-02-26
PRIOR — 2025-03-03
ADDED
At February 20, 2026, there were 45,370,171 shares of the registrant s common stock outstanding.
Overview We are a biopharmaceutical company focusing on developing, manufacturing, and commercializing technically challenging generic and proprietary injectable, inhalation, and intranasal products, as well as active pharmaceutical ingredient, or API products.
We currently manufacture and sell over 25 prescription pharmaceutical products, and an over-the-counter product, Primatene MIST .
In August 2025, the FDA approved our iron sucrose injection, USP 50mg/2.5mL, 100mg/5mL, and 200mg/10mL in single-dose vials, which we launched in the August 2025.
In December 2025, the FDA approved our teriparatide injection, USP 560mcg/2.24mLsingle-patient-use prefilled pen, which we launched in the December 2025.
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REMOVED
At February 25, 2025, there were 47,650,121 shares of the registrant s common stock outstanding.
Overview We are a bio-pharmaceutical company focusing primarily on developing, manufacturing, marketing, and selling technically challenging generic and proprietary injectable, inhalation, and intranasal products, as well as insulin active pharmaceutical ingredient, or insulin API products.
We currently manufacture and sell over 25 products, the overwhelming majority of which are prescription pharmaceuticals.
Since December 2018, we have sold our patented Primatene MIST using a new hydrofluoroalkanes, or HFA, formulation as our sole over-the-counter product.
In March 2023, the FDA approved our naloxone hydrochloride nasal spray 4mg, REXTOVY TM , utilizing our proprietary device, which we launched in May 2024.
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