NDC 68151-0527 Norpace
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68151 - Carilion Materials Management
- 68151-0527 - Norpace
Product Characteristics
GREEN (C48329 - LIGHT GREEN)
Product Packages
NDC Code 68151-0527-3
Package Description: 1 CAPSULE, GELATIN COATED in 1 PACKAGE
Product Details
What is NDC 68151-0527?
What are the uses for Norpace?
Which are Norpace UNII Codes?
The UNII codes for the active ingredients in this product are:
- DISOPYRAMIDE PHOSPHATE (UNII: N6BOM1935W)
- DISOPYRAMIDE (UNII: GFO928U8MQ) (Active Moiety)
Which are Norpace 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:
- STARCH, CORN (UNII: O8232NY3SJ)
- ETHYLCELLULOSES (UNII: 7Z8S9VYZ4B)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- GELATIN (UNII: 2G86QN327L)
- SHELLAC (UNII: 46N107B71O)
- SUCROSE (UNII: C151H8M554)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FD&C RED NO. 3 (UNII: PN2ZH5LOQY)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
What is the NDC to RxNorm Crosswalk for Norpace?
- RxCUI: 209692 - Norpace 150 MG Oral Capsule
- RxCUI: 209692 - disopyramide 150 MG Oral Capsule [Norpace]
- RxCUI: 209692 - Norpace (as disopyramide phosphate) 150 MG Oral Capsule
- RxCUI: 309960 - disopyramide phosphate 150 MG Oral Capsule
- RxCUI: 309960 - disopyramide 150 MG Oral Capsule
* 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".