NDC 43386-140 Methylergonovine Maleate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43386 - Lupin Pharmaceuticals,inc.
- 43386-140 - Methylergonovine Maleate
Product Characteristics
Product Packages
Product Details
What is NDC 43386-140?
What are the uses for Methylergonovine Maleate?
Which are Methylergonovine Maleate UNII Codes?
The UNII codes for the active ingredients in this product are:
- METHYLERGONOVINE MALEATE (UNII: IR84JPZ1RK)
- METHYLERGONOVINE (UNII: W53L6FE61V) (Active Moiety)
Which are Methylergonovine Maleate 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:
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POVIDONE K30 (UNII: U725QWY32X)
- STARCH, CORN (UNII: O8232NY3SJ)
- GELATIN (UNII: 2G86QN327L)
- ACACIA (UNII: 5C5403N26O)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- TARTARIC ACID (UNII: W4888I119H)
- STEARIC ACID (UNII: 4ELV7Z65AP)
What is the NDC to RxNorm Crosswalk for Methylergonovine Maleate?
- RxCUI: 996824 - methylergonovine maleate 0.2 MG Oral Tablet
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Patient Education
Methylergonovine
Methylergonovine belongs to a class of drugs called ergot alkaloids. Methylergonovine is used to prevent or treat bleeding from the uterus that can happen after childbirth or an abortion. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
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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".