NDC 21695-880 Methyldopa
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 21695 - Rebel Distributors Corp
- 21695-880 - Methyldopa
Product Characteristics
13 MM
Z;2932
Product Packages
NDC Code 21695-880-60
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE
Product Details
What is NDC 21695-880?
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 (UNII: 56LH93261Y) (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 (UNII: 2968PHW8QP)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- ETHYLCELLULOSE (10 MPA.S) (UNII: 3DYK7UYZ62)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- METHYLCELLULOSE (15 CPS) (UNII: NPU9M2E6L8)
- POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- CALCIUM SULFATE (UNII: WAT0DDB505)
- HYDROXYPROPYL CELLULOSE (UNII: RFW2ET671P)
- TALC (UNII: 7SEV7J4R1U)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
What is the NDC to RxNorm Crosswalk for Methyldopa?
- RxCUI: 197956 - methyldopa 250 MG Oral Tablet
- RxCUI: 197958 - methyldopa 500 MG Oral Tablet
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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".