Meclofenamate Sodium Capsules, Usp 50 mg Bottle Label (Image 01)
Meclofenamate Sodium Capsule
Product Images NDC 0378-3000
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This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Meclofenamate Sodium (NDC 0378-3000). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Mylan 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.
Meclofenamate Sodium Capsules, Usp 100 mg Bottle Label (Image 02)
Scattergram Of Menstrual Flow Average Of Two Periods On Each Treatment Of 55 Women From Three Clinical Trials (Image 03)
This appears to be a prescription medication called Meclofenamate Sodium, USP monohydrate, which is available in capsule form. The usual dosage is between 200 and 400 mg. The medication should be stored in a cool, dry place away from light, in a tightly sealed, light-resistant container. The accompanying Medication Guide should be given to each patient by the pharmacist. There is additional information on the packaging related to proper storage and handling of the medication.*
Meclofenamate Structural Formula (Image 04)
Each capsule of Meclofenamate Sodium Capsules, USP contains 100 mg of meclofenamate acid. The usual recommended dosage is 200 to 400 mg per day, split into three or four equal doses. Full prescribing information can be found in the package insert. This medication should be kept out of the reach of children, stored between 20° and 26°C (68°F and 77°F) in a controlled room temperature environment and away from light and moisture. It should be dispensed in a tightly closed, light-resistant container with child-resistant closure. The code NHIDRUES/25/NKD/BY should be used for dispensing purposes. The text suggests that Mylan Pharmaceuticals Inc. produced this medication, and it was made in India. The GTIN is 000000000000, and the lot number is X000, with an expiry date of MM YYYY. If you are dispensing this medication, it is essential to provide the accompanying medication guide to the patient.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.
