Chemical Structure (Phenobarbital 01)
Chemical structure of Phenobarbital showing a barbiturate ring with ethyl and phenyl substituents.*
Phenobarbital Tablet
Product Images NDC 69367-442
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 Phenobarbital (NDC 69367-442). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Westminster Pharmaceuticals, Llc, 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
Principal Display Panel (15 mg Tablet Bottle Label)
Label for Phenobarbital Tablets, USP 15 mg oral tablets, packaged as 100 tablets. The label includes the drug schedule (C-IV) and states the product is prescription only (Rx Only). It is manufactured for Westminster Pharmaceuticals, LLC. The label also contains storage instructions, a habit-forming warning, dosage notice to read full prescribing information, and a barcode with NDC 69367-438-01.*
Principal Display Panel (16.2 mg Tablet Bottle Label)
Phenobarbital 16.2 mg oral tablets label by Westminster Pharmaceuticals, LLC. The label notes each tablet contains 16.2 mg Phenobarbital USP, lists storage and handling instructions, a habit-forming warning, and indicates the package contains 100 tablets. It includes an NDC number and a barcode.*
Principal Display Panel (30 mg Tablet Bottle Label)
Phenobarbital tablets, USP 30 mg oral tablets label from Westminster Pharmaceuticals, LLC. The label states a quantity of 100 tablets and includes a warning that the drug may be habit forming. It provides storage instructions and a notice to read the package insert for full prescribing information. The label features the NDC 69367-440-01 and a barcode.*
Principal Display Panel (32.4 mg Tablet Bottle Label)
Label for Phenobarbital tablets, USP 32.4 mg, oral tablets. The package contains 100 tablets and is labeled for prescription use only (Rx Only). Manufactured for Westminster Pharmaceuticals, LLC, Nashville, TN. The label includes dosage instructions, storage conditions (20°C to 25°C), and a habit-forming warning.*
Principal Display Panel (60 mg Tablet Bottle Label)
Phenobarbital Tablets, USP 60 mg oral tablets label. Contains 100 tablets per container. The label is from Westminster Pharmaceuticals, LLC, Nashville, TN. It includes warnings, storage instructions, and an NDC number (69367-442-01) with barcode and GTIN.*
Principal Display Panel (64.8 mg Tablet Bottle Label)
Label for Phenobarbital Tablets, USP 64.8 mg, manufactured by Westminster Pharmaceuticals, LLC. The label states the tablet strength, quantity of 100 tablets, and prescription-only status. Includes storage instructions, a habit-forming warning, NDC 69367-443-01, and barcode with GTIN 00369367443012.*
Principal Display Panel (97.2 mg Tablet Bottle Label)
Phenobarbital Tablets USP 97.2 mg oral tablets label by Westminster Pharmaceuticals, LLC. The label lists dosage strength, includes storage instructions, a habit-forming warning, the NDC number 69367-444-01, and states package contains 100 tablets. Barcode and GTIN 00369367444019 are visible.*
Principal Display Panel (100 mg Tablet Bottle Label)
Label for Phenobarbital Tablets, USP 100 mg oral tablets from Westminster Pharmaceuticals, LLC. The label indicates 100 tablets per container and includes a warning about habit forming. It advises storing at 20°C to 25°C in a child-resistant container and refers to the package insert for full dosage and administration instructions.*
* 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.
