NDC 42254-351 Methyldopa
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 42254 - Rebel Distributors Corp
- 42254-351 - Methyldopa
Product Characteristics
Product Packages
NDC Code 42254-351-90
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE
Product Details
What is NDC 42254-351?
What are the uses for Methyldopa?
Which are Methyldopa UNII Codes?
The UNII codes for the active ingredients in this product are:
- METHYLDOPA (UNII: 56LH93261Y)
- METHYLDOPA ANHYDROUS (UNII: M4R0H12F6M) (Active Moiety)
Which are Methyldopa 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:
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- ETHYLCELLULOSES (UNII: 7Z8S9VYZ4B)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- METHYLCELLULOSE (400 MPA.S) (UNII: O0GN6F9B2Y)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- CALCIUM SULFATE (UNII: WAT0DDB505)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- HYDROXYPROPYL CELLULOSE (TYPE H) (UNII: RFW2ET671P)
- TALC (UNII: 7SEV7J4R1U)
What is the NDC to RxNorm Crosswalk for Methyldopa?
- RxCUI: 197956 - methyldopa 250 MG Oral Tablet
* Please review the disclaimer below.
[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".