NDC 69874-992 Tofranil
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69874 - Thompson Medical Solutions Llc
- 69874-992 - Tofranil
Product Characteristics
Product Packages
NDC Code 69874-992-01
Package Description: 100 TABLET, SUGAR COATED in 1 BOTTLE
Product Details
What is NDC 69874-992?
What are the uses for Tofranil?
Which are Tofranil UNII Codes?
The UNII codes for the active ingredients in this product are:
- IMIPRAMINE HYDROCHLORIDE (UNII: BKE5Q1J60U)
- IMIPRAMINE (UNII: OGG85SX4E4) (Active Moiety)
Which are Tofranil 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:
- CALCIUM PHOSPHATE, UNSPECIFIED FORM (UNII: 97Z1WI3NDX)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- DOCUSATE SODIUM (UNII: F05Q2T2JA0)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
- POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- SUCROSE (UNII: C151H8M554)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Tofranil?
- RxCUI: 835593 - imipramine HCl 10 MG Oral Tablet
- RxCUI: 835593 - imipramine hydrochloride 10 MG Oral Tablet
- RxCUI: 835596 - Tofranil 10 MG Oral Tablet
- RxCUI: 835596 - imipramine hydrochloride 10 MG Oral Tablet [Tofranil]
* 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".