Baclofen Tablet
Product Images NDC 71930-066

10 FDA label images from Eywa Pharma Inc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Baclofen (NDC 71930-066). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Eywa Pharma 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

Baclofen 10mg 1000s

Baclofen 10mg 1000s
Label for Baclofen Tablets, USP 10 mg oral tablets, distributed by Eywa Pharma Inc. The label states the NDC number 71930-006-13 and packaging contains 1000 tablets. Storage and dispensing instructions, dosage reference, and a child-resistant closure notice are also included.*
FDA Label Image

Baclofen 10mg 100s

Baclofen 10mg 100s
Label for Baclofen Tablets, USP, 10 mg strength, oral tablet form, by Eywa Pharma Inc. The label includes the NDC 71930-006-12, a barcode, and states the package size as 100 tablets. It also provides storage instructions and dispensing information.*
FDA Label Image

Baclofen 10mg 500s

Baclofen 10mg 500s
Label for Baclofen Tablets, USP 10 mg by Eywa Pharma Inc. The label shows 500 tablets with a barcode, NDC 71930-006-52, and storage instructions at 20° to 25°C. The label also includes dispensing and safety information and the distributor address in Princeton, NJ.*
FDA Label Image

Baclofen 20mg 1000s

Baclofen 20mg 1000s
Label for Baclofen Tablets, USP 20 mg oral tablets, distributed by Eywa Pharma Inc. The label states the NDC 71930-007-13 and indicates a package size of 1000 tablets. It includes storage instructions at 20°C to 25°C and a note to dispense in a child-resistant container. The label also features the Eywa Pharma logo.*
FDA Label Image

Baclofen 20mg 100s

Baclofen 20mg 100s
Baclofen Tablets, USP 20 mg oral tablets packaging label showing 100 tablets per container. The label includes NDC number 71930-007-12, storage instructions (20°C to 25°C), dispensing guidance, and distribution by Eywa Pharma Inc, Princeton, NJ. The label indicates prescription use only.*
FDA Label Image

Baclofen 20mg 500s

Baclofen 20mg 500s
Label for Baclofen Tablets, USP 20 mg oral tablets manufactured by Eywa Pharma Inc. The label indicates 500 tablets per container with NDC 71930-007-52. Storage instructions specify 20°C to 25°C, with additional dispensing and safety warnings.*
FDA Label Image

Baclofen 5mg 1000s

Baclofen 5mg 1000s
Label for Baclofen Tablets USP, 5 mg strength, oral tablets. The label includes the NDC 71930-066-13, barcode, and states 1000 tablets per container. It is distributed by Eywa Pharma Inc in Princeton, NJ. Storage instructions and dosage directions advising to see package insert are also present.*
FDA Label Image

Baclofen 5mg 100s

Baclofen 5mg 100s
Label for Baclofen Tablets, USP 5 mg oral tablets by Eywa Pharma Inc. The label indicates 100 tablets per bottle with NDC 71930-066-12. It includes storage instructions (20°C to 25°C), dispensing details, and child-resistant closure warning. The label also displays the barcode and distributor address in Princeton, NJ.*
FDA Label Image

Baclofen 5mg 500s

Baclofen 5mg 500s
Baclofen Tablets USP 5 mg oral tablets label from Eywa Pharma Inc. The label includes the NDC 71930-066-52 and indicates a package size of 500 tablets. It provides storage instructions, dosage caution, and child-resistant closure information, along with distributor details in Princeton, NJ.*
FDA Label Image

Baclofen Str

Baclofen Str
Chemical structure of Baclofen, showing a phenyl ring with a chlorine atom and the associated side chain containing an amino and carboxylic acid group.*

* 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.