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Amneal Pharmaceuticals, Inc. AMRX Affordable Medicines — Regulatory fees
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Where this comes from
Reported directly by Amneal Pharmaceuticals, Inc. in its filing.
Tagged under the XBRL concept amrx:RegulatoryFeesExpense.
The source filing: Amneal Pharmaceuticals, Inc.’s 10-Q, filed August 6, 2026.
- Filed
- Aug 6, 2026, 5:19 PM EDT
- Fiscal quarter
- Q2 FY2026
- Calendar quarter
- Q2 2026
- Accession
- 0001723128-26-000031
| Line item | Three Months Ended June 30, 2026 / Affordable Medicines | Three Months Ended June 30, 2026 / Specialty | Three Months Ended June 30, 2025 / Affordable Medicines | Three Months Ended June 30, 2025 / Specialty |
|---|---|---|---|---|
| Employee compensation and benefits | $12,016 | $1,326 | $14,693 | $1,279 |
| Materials and supplies | 8,796 | 1,022 | 8,108 | 450 |
| Product development and studies (1) | (89) | 2,615 | 756 | 2,371 |
| In-licensing and upfront milestones | 3,500 | — | 6,350 | — |
| Facilities costs | 1,479 | 30 | 1,793 | 735 |
| Regulatory fees | 1,334 | — | 2,932 | — |
| Other (2) | 5,987 | 1,001 | 7,267 | 1,230 |
| Total | $33,023 | $5,994 | $41,899 | $6,065 |
Item 1. Financial Statements (Unaudited)
FAQ
- What is Amneal Pharmaceuticals, Inc.'s affordable medicines — regulatory fees?
- Amneal Pharmaceuticals, Inc. (AMRX) reported affordable medicines — regulatory fees of $1.33M in Q2 2026.
- How has Amneal Pharmaceuticals, Inc.'s affordable medicines — regulatory fees changed year-over-year?
- Amneal Pharmaceuticals, Inc.'s affordable medicines — regulatory fees decreased by 54.5% year-over-year, from $2.93M to $1.33M.
- What is the long-term trend for Amneal Pharmaceuticals, Inc.'s affordable medicines — regulatory fees?
- Over 3 years (2022 to 2025), Amneal Pharmaceuticals, Inc.'s affordable medicines — regulatory fees has grown at a 4.9% compound annual growth rate (CAGR), from $5.54M to $6.4M.
- What does affordable medicines — regulatory fees mean?
- Represents the costs associated with compliance, filing fees, and regulatory oversight required by health authorities to maintain product approvals. These costs are essential for market access and reflect the regulatory burden of the segment's portfolio.
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