Abacavir Tablet
Product Images NDC 31722-557

5 FDA label images from Camber Pharmaceuticals, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Abacavir (NDC 31722-557). 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.

Product Images & Figures Index

FDA Label Image

Abacavircarton (Abacavircarton)

Abacavircarton (Abacavircarton)
Packaging label for Abacavir Tablets USP 300 mg oral tablets by Camber Pharmaceuticals, Inc. The label indicates 60 tablets per bottle and includes the NDC 31722-557-60. It features dispensing instructions, storage conditions, contact information, and a barcode. The manufacturer is listed as Camber Pharmaceuticals in Piscataway, NJ.*
FDA Label Image

Abacavircontaier60s (Abacavircontainer60s)

Abacavircontaier60s (Abacavircontainer60s)
Label for Abacavir Tablets USP 300 mg oral tablets by Camber Pharmaceuticals, Inc. The label includes NDC 31722-557-60, quantity of 60 tablets, and mentions the active ingredient abacavir sulfate equivalent to 300 mg abacavir per tablet. It also displays storage instructions, a U.S. contact number, manufacturing information specifying production by Hetero Labs Limited in Hyderabad, India, and a barcode.*
FDA Label Image

Abacavirstructure1

Abacavirstructure1
Chemical structure diagram of abacavir sulfate, indicating two abacavir molecules complexed with sulfuric acid (H2SO4). The structure features fused ring systems and functional groups characteristic of abacavir.*
FDA Label Image

Camber1

Camber1
FDA Label Image

Camber2

Camber2

* 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.