NDC 62034-021 Duloxetine Delayed-release
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 62034 - Blenheim Pharmacal, Inc.
- 62034-021 - Duloxetine
Product Characteristics
WHITE (C48325)
YELLOW (C48330 - OCHRE)
19 MM
B;748
Product Packages
NDC Code 62034-021-77
Package Description: 100 BLISTER PACK in 1 BOX, UNIT-DOSE / 1 CAPSULE, DELAYED RELEASE PELLETS in 1 BLISTER PACK (62034-021-11)
Product Details
What is NDC 62034-021?
What are the uses for Duloxetine Delayed-release?
Which are Duloxetine Delayed-release UNII Codes?
The UNII codes for the active ingredients in this product are:
- DULOXETINE HYDROCHLORIDE (UNII: 9044SC542W)
- DULOXETINE (UNII: O5TNM5N07U) (Active Moiety)
Which are Duloxetine Delayed-release 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:
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A (UNII: NX76LV5T8J)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- AMMONIA (UNII: 5138Q19F1X)
- POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
- SHELLAC (UNII: 46N107B71O)
- SUCROSE (UNII: C151H8M554)
- STARCH, CORN (UNII: O8232NY3SJ)
- GELATIN (UNII: 2G86QN327L)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
What is the NDC to RxNorm Crosswalk for Duloxetine Delayed-release?
- RxCUI: 596930 - DULoxetine 30 MG Delayed Release Oral Capsule
- RxCUI: 596930 - duloxetine 30 MG Delayed Release Oral Capsule
- RxCUI: 596930 - duloxetine 30 MG (as duloxetine HCl 33.7 MG) Delayed Release Oral Capsule
- RxCUI: 596934 - DULoxetine 60 MG Delayed Release Oral Capsule
- RxCUI: 596934 - duloxetine 60 MG Delayed Release 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".