NDC 21695-443 Next Choice
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 21695 - Rebel Distributors Corp.
- 21695-443 - Next Choice
Product Characteristics
Product Packages
NDC Code 21695-443-02
Package Description: 1 TABLET in 1 BLISTER PACK
Product Details
What is NDC 21695-443?
What are the uses for Next Choice?
Which are Next Choice UNII Codes?
The UNII codes for the active ingredients in this product are:
- LEVONORGESTREL (UNII: 5W7SIA7YZW)
- LEVONORGESTREL (UNII: 5W7SIA7YZW) (Active Moiety)
Which are Next Choice 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:
- COLLOIDAL SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- STARCH, CORN (UNII: O8232NY3SJ)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POVIDONE (UNII: FZ989GH94E)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
What is the NDC to RxNorm Crosswalk for Next Choice?
- RxCUI: 259218 - levonorgestrel 0.75 MG 2 Count Oral Tablet Pack
- RxCUI: 259218 - levonorgestrel 0.75 MG Oral Tablet
- RxCUI: 763088 - {2 (levonorgestrel 0.75 MG Oral Tablet) } Pack
- RxCUI: 763088 - Levonorgest 0.75 MG (2) Oral Tablet
- RxCUI: 854861 - {2 (levonorgestrel 0.75 MG Oral Tablet) } Pack [Next Choice]
* 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".