Prednisone
Product Images NDC 67296-0138

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Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Prednisone (NDC 67296-0138). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Redpharm Drug, 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

67296 0138

67296 0138
This text appears to be a collection of different labels for medication. They mention the name of the drug (PREDNISONE), its dosage (20MG), number of tablets, lot number, expiration date, manufacturer (Watson Pharma Private Limited), distributor (Redpharm Drug), and storage instructions. The labels also include an NDC (National Drug Code).*
FDA Label Image

Serialized Labels (Sdistributi19020814510 0001)

Serialized Labels (Sdistributi19020814510 0001)
This is a description of Prednisone, a medication that requires a prescription. It comes in the form of tablets and is available in two dosages, 10mg and 20mg. The usual adult dosage should be consulted from the package insert. The medication should be stored at a controlled room temperature between 20-25C (68-77F). The manufacturer is identified as Watson Pharma Private Limited based in Salcette Goa, India. The medication is distributed in the US by Redpharm Drug based in Eden Prairie, Minnesota. The NDC codes for both dosages are given, specifically 67296-0138-1 for 10mg and 67296-0138-2 for 20mg. The lot number for the 10mg dosage is 20862AX2 with an expiration date of 06/20, while the lot number for the 20mg dosage is not given.*
FDA Label Image

Sdistributi19043014320 0001

Sdistributi19043014320 0001
PREDNISONE is a prescription medicine with NDC code 67296-0138-3. It contains twenty tablets, each containing 20mg of prednisone. The usual adult dosage is available in the package insert. It should be stored at controlled room temperature between 20-25 C (68-77 F). The medicine is manufactured by Watson Pharma Private Limited located in Verna Salcette Goa 403 722 India. The lot number is 20862AX5 with an expiration date of 06/20. It is distributed by Redpharm Drug in Eden Prairie, MN 55344 with SIN220430.*
FDA Label Image

Structural Formula For Prednisone (Image 1)

FDA Label Image

Ndc 0591-5052-10 Prednisone Tablets, Usp 5 mg 1,000 Tablets Rx Only (Image 2)

Ndc 0591-5052-10 Prednisone Tablets, Usp 5 mg 1,000 Tablets Rx Only (Image 2)
PredniSONE Tablets is a prescription medicine that contains 5mg of Prednisone USP (anhydrous) in each tablet. It is dispensed in a container with a child-resistant closure. The medication is used based on the instructions provided in the package insert. The tablets are manufactured by Watson Pharma Private Limited and distributed by Actavis Pharma, Inc. The medicine should be stored between 20°C to 25°C (68°F to 77°F), as per USP Controlled Room Temperature regulations. The NDC number for this medication is 0591-5052-10.*
FDA Label Image

Ndc 0591-5442-10 Prednisone Tablets, Usp 10 mg 1,000 Tablets Rx Only (Image 3)

Ndc 0591-5442-10 Prednisone Tablets, Usp 10 mg 1,000 Tablets Rx Only (Image 3)
PredniSONE is a prescription medication available in a bottle of 1,000 tablets. Each tablet contains 10mg anhydrous Prednisone USP manufactured by Watson Pharma Private Limited. It is distributed by Actavis Pharma, Inc. in Parsippany, NJ. Typical usage should be followed as per the package insert, and the medication should be stored in a child-resistant, well-closed bottle at temperatures of 20-25°C (68-77°F). Additional information on prescribing can be obtained from the package insert. Lot information is below, and other details on the medication may be found on the label.*
FDA Label Image

Ndc 0591-5443-10 Prednisone Tablets, Usp 20 mg 1,000 Tablets Rx Only (Image 4)

Ndc 0591-5443-10 Prednisone Tablets, Usp 20 mg 1,000 Tablets Rx Only (Image 4)
NDC 0591-5443-10 is for PredniSONE tablets, USP, containing 20 mg of Prednisone, USP (anhydrous). It is available as a prescription drug with 1,000 tablets per container. The package insert provides dosage and full prescribing information for the usual dosage. It should be stored in a controlled room temperature of 20°to 25°C (68°to 77°F), and dispensed in a well-closed container with child-resistant closure. The tablets are manufactured by Watson Pharma Private Limited, Goa, India, and distributed by Actavis Pharma, Inc., Parsippany, NJ, USA.*
FDA Label Image

Ndc 0591-5052-21 Prednisone Tablets, Usp 5 mg 21 Tablets (Image 5)

Ndc 0591-5052-21 Prednisone Tablets, Usp 5 mg 21 Tablets (Image 5)
This is a medication package for PredniSONE Tablets, USP by Actavis. The package contains 21 tablets and the dosage is to be prescribed by a physician. It should be stored at temperatures between 20°C-25°C, in a cool and dry place. The medication should be taken with caution and under the observation of a physician. There is a pharmacy label on the package for identification purposes.*
FDA Label Image

Ndc 0591-5442-21 Prednisone Tablets, Usp 10 mg 21 Tablets (Image 6)

Ndc 0591-5442-21 Prednisone Tablets, Usp 10 mg 21 Tablets (Image 6)
This is a product label for PredniSONE Tablets, USP, manufactured by Actavis. It is a prescription medication, indicated for various inflammatory conditions. The label provides instructions for dosage, storage, precautions, and warnings. The package contains 21 tablets and is for single-use only. The label is for pharmacy use only and contains special instructions regarding proper labeling to be used on prescription containers.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.