====== Product Detail ======

The product detail screen shows complete information for an NDC product. Access it by tapping any result in Search or Browse, or after scanning a barcode.

===== Product Information =====

The top section displays:

  * **Brand name** — The proprietary/trade name
  * **Generic name** — The nonproprietary name
  * **NDC** — The product NDC code
  * **Labeler** — Manufacturer or distributor
  * **Dosage form** — Tablet, capsule, injection, etc.
  * **Route** — How the drug is administered
  * **DEA Schedule** — Controlled substance schedule (if applicable)
  * **Marketing category** — NDA, ANDA, OTC monograph, etc.
  * **Marketing start date** — When the product was first marketed
  * **Application number** — FDA application reference
  * **Internal ID** — Database row identifier

===== Packages =====

The Packages section lists all package configurations for the product. Each package shows:

  * **Package NDC** — The 10-digit and 11-digit formatted NDC
  * **Description** — Full package description
  * **Package levels** — Hierarchical breakdown (e.g., 100 tablets in 1 bottle in 1 carton)

Products may have multiple packages representing different pack sizes or configurations.

===== Active Ingredients =====

Lists each active ingredient with:

  * **Substance name** — The ingredient name
  * **Strength** — Numeric strength and unit (e.g., "20 mg")

===== Pharmacological Classes =====

Shows the drug's pharmacological and therapeutic classifications, including:

  * **EPC** — Established Pharmacologic Class
  * **Chemical/Ingredient** — Chemical structure classification
  * **MoA** — Mechanism of Action
  * **PE** — Physiologic Effect

===== Report an Issue =====

At the bottom of every product detail page, there is a **Report an Issue** button. This opens an email to support with the product name and NDC pre-filled, making it easy to report data issues or errors.