NDC 21695-952 Depo-medrol
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 21695 - Rebel Distributors Corp
- 21695-952 - Depo-medrol
Product Packages
NDC Code 21695-952-05
Package Description: 5 mL in 1 VIAL, MULTI-DOSE
Product Details
What is NDC 21695-952?
What are the uses for Depo-medrol?
Which are Depo-medrol UNII Codes?
The UNII codes for the active ingredients in this product are:
- METHYLPREDNISOLONE ACETATE (UNII: 43502P7F0P)
- METHYLPREDNISOLONE (UNII: X4W7ZR7023) (Active Moiety)
Which are Depo-medrol Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- SODIUM PHOSPHATE, MONOBASIC (UNII: 3980JIH2SW)
- SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
What is the NDC to RxNorm Crosswalk for Depo-medrol?
- RxCUI: 1358610 - methylPREDNISolone acetate 40 MG/ML Injectable Suspension
- RxCUI: 1358610 - methylprednisolone acetate 40 MG/ML Injectable Suspension
- RxCUI: 1358612 - DEPO-Medrol 40 MG/ML Injectable Suspension
- RxCUI: 1358612 - methylprednisolone acetate 40 MG/ML Injectable Suspension [Depo-Medrol]
- RxCUI: 1358612 - Depo-Medrol 40 MG/ML Injectable Suspension
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".