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.

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

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.

Lists each active ingredient with:

• Substance name — The ingredient name
• Strength — Numeric strength and unit (e.g., “20 mg”)

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

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.