Phenobarbital Tablet
Product Images NDC 51672-5332

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Phenobarbital (NDC 51672-5332). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sun Pharmaceutical Industries, 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

Chemical Structure (Phenobarbital 01)

Chemical structure diagram of Phenobarbital showing its molecular arrangement with labeled atoms and bonds, including characteristic rings and functional groups.*

FDA Label Image

Principal Display Panel (16.2 mg Tablet Bottle Label)

Phenobarbital Tablets USP 16.2 mg oral tablets packaged in a label from Sun Pharmaceutical Industries, Inc. The label indicates a prescription-only drug with a net content of 100 tablets. It includes a warning that the drug may be habit-forming and instructions to keep medication out of children’s reach.*

FDA Label Image

Principal Display Panel (32.4 mg Tablet Bottle Label)

Label for Phenobarbital Tablets USP 32.4 mg by Sun Pharmaceutical Industries, Inc. The oral tablet packaging states habit-forming warning and prescription only status. The label includes storage instructions, manufacturer details for Taro Pharmaceuticals U.S.A., Inc., and shows a net content of 100 tablets with identifying barcodes and NDC number.*

FDA Label Image

Principal Display Panel (64.8 mg Tablet Bottle Label)

Phenobarbital tablets, USP 64.8 mg oral tablets packaged in a container labeled to contain 100 tablets. The label includes a caution that the drug may be habit forming and indicates prescription use only. The manufacturer listed is Sun Pharmaceutical Industries, Inc., with references to storage conditions and usage instructions.*

FDA Label Image

Principal Display Panel (97.2 mg Tablet Bottle Label)

Phenobarbital 97.2 mg tablets label showing the product name, strength, and dosage form as oral tablets. The label includes storage instructions, a warning about habit forming, prescription only status, and a net content of 100 tablets. The labeler is Taro Pharmaceuticals U.S.A., Inc.*

FDA Label Image

Principal Display Panel (15 mg Tablet Bottle Label)

Phenobarbital 15 mg oral tablets label by Sun Pharmaceutical Industries, Inc. The label shows 'PHENOBARBITAL TABLETS, USP' with strength 15 mg, a caution warning that the drug may be habit forming, and prescription only status. It indicates a net content of 100 tablets and includes manufacturer details for Taro Pharmaceuticals U.S.A., Inc.*

FDA Label Image

Principal Display Panel (30 mg Tablet Bottle Label)

Phenobarbital tablets, USP 30 mg oral tablets packaging label. The label includes the strength of 30 mg, prescription-only status (Rx only), a warning about habit forming potential, net contents of 100 tablets, and is manufactured by Sun Pharmaceutical Industries, Inc. It also includes storage instructions and a barcode.*

FDA Label Image

Principal Display Panel (60 mg Tablet Bottle Label)

Phenobarbital tablets, USP 60 mg oral tablets label. The label indicates the product contains 60 mg of phenobarbital per tablet, with a warning that the drug may be habit forming. It is Rx only and contains 100 tablets. The label also includes storage instructions, manufacturer information for Taro Pharmaceuticals U.S.A., Inc., and a barcode.*

FDA Label Image

Principal Display Panel (100 mg Tablet Bottle Label)

Phenobarbital 100 mg oral tablets label showing the product name, strength, and USP designation. The label includes warnings about habit forming potential, Rx only status, net content of 100 tablets, and storage instructions. Manufactured for Taro Pharmaceuticals U.S.A., Inc., with barcode and NDC number visible.*

* 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.