Tolterodine Tartrate Capsule, Extended Release
Product Images NDC 31722-608

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Tolterodine Tartrate (NDC 31722-608). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Camber Pharmaceuticals, Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Tolterodinetartrate2mg30slabel (Tolterodinetartrate2mg30slabel)

Tolterodinetartrate2mg30slabel (Tolterodinetartrate2mg30slabel)
Label for Tolterodine Tartrate Extended-release Capsules 2 mg by Camber Pharmaceuticals, Inc. The label includes storage instructions (20° to 25°C), a barcode, manufacturer information, and a 30-capsule count. It also features a pharmacist advisory to dispense the patient information leaflet separately.*
FDA Label Image

Tolterodinetartrate2mg500slabel (Tolterodinetartrate2mg500slabel)

Tolterodinetartrate2mg500slabel (Tolterodinetartrate2mg500slabel)
Tolterodine Tartrate extended-release capsules label by Camber Pharmaceuticals, Inc. The label indicates 2 mg strength oral capsules, packaged as 500 capsules. It includes storage instructions, barcode, U.S. contact number, and distributor information from Hetero Labs Limited, India. The label highlights the prescription-only status and pharmacist dispensing instructions.*
FDA Label Image

Tolterodinetartrate2mg90slabel (Tolterodinetartrate2mg90slabel)

Tolterodinetartrate2mg90slabel (Tolterodinetartrate2mg90slabel)
Label for Tolterodine Tartrate Extended-release Capsules 2 mg by Camber Pharmaceuticals, Inc. The label indicates 90 capsules per container with NDC 31722-607-90. Storage instructions specify 20° to 25°C and protection from light. Manufacturer contact and licensing details are included, with emphasis on pharmacist dispensing instructions.*
FDA Label Image

Tolterodinetartrate4mg30slabel (Tolterodinetartrate4mg30slabel)

Tolterodinetartrate4mg30slabel (Tolterodinetartrate4mg30slabel)
Label for Tolterodine Tartrate Extended-release Capsules, 4 mg, by Camber Pharmaceuticals, Inc. The label indicates a package of 30 capsules. Storage instructions recommend 20 to 25°C (68 to 77°F) in a controlled room temperature. The product is prescription-only and includes a pharmacist's dispensing note. It is manufactured by Hetero Labs Limited, India.*
FDA Label Image

Tolterodinetartrate4mg500slabel (Tolterodinetartrate4mg500slabel)

Tolterodinetartrate4mg500slabel (Tolterodinetartrate4mg500slabel)
Label for Tolterodine Tartrate extended-release capsules 4 mg by Camber Pharmaceuticals, Inc. The label states the product contains 4 mg of tolterodine tartrate per capsule, with a package size of 500 capsules. Additional information includes storage instructions, a pharmacist dispensing notice, manufacturer details, and the NDC 31722-608-05.*
FDA Label Image

Tolterodinetartrate4mg90slabel (Tolterodinetartrate4mg90slabel)

Tolterodinetartrate4mg90slabel (Tolterodinetartrate4mg90slabel)
Label for Tolterodine Tartrate Extended-release Capsules 4 mg by Camber Pharmaceuticals, Inc. The label displays the NDC 31722-608-90 and indicates a package size of 90 capsules. Storage instructions specify 20° to 25°C, protect from light. The label also includes a U.S. contact number and notes the product is Rx only.*
FDA Label Image

Tolterodinetartratestructure (Tolterodinetartratestructure)

Tolterodinetartratestructure (Tolterodinetartratestructure)
Chemical structure of Tolterodine Tartrate, showing its molecular arrangement including aromatic rings, hydroxyl group, and tertiary amine, along with the tartrate salt component.*
FDA Label Image

Camberlogo1 (Camberlogo1)

FDA Label Image

Camberlogo2 (Camberlogo2)

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.