NDC 55648-926 Enalapril Maleate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 55648 - Wockhardt Limited
- 55648-926 - Enalapril Maleate
Product Characteristics
ORANGE (C48331 - LIGHT SALMON)
BROWN (C48332 - LIGHT BEIGE)
8 MM
W;924
W;925
W;926
1
Product Packages
NDC Code 55648-926-01
Package Description: 90 TABLET in 1 BOTTLE
NDC Code 55648-926-02
Package Description: 100 TABLET in 1 BOTTLE
NDC Code 55648-926-03
Package Description: 1000 TABLET in 1 BOTTLE
NDC Code 55648-926-07
Package Description: 10 BLISTER PACK in 1 CARTON / 10 TABLET in 1 BLISTER PACK
NDC Code 55648-926-09
Package Description: 40000 TABLET in 1 DRUM
NDC Code 55648-926-10
Package Description: 8000 TABLET in 1 DRUM
Product Details
What is NDC 55648-926?
What are the uses for Enalapril Maleate?
Which are Enalapril Maleate UNII Codes?
The UNII codes for the active ingredients in this product are:
- ENALAPRIL MALEATE (UNII: 9O25354EPJ)
- ENALAPRILAT ANHYDROUS (UNII: Q508Q118JM) (Active Moiety)
Which are Enalapril Maleate 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:
- ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
- HYPROMELLOSE 2910 (6 MPA.S) (UNII: 0WZ8WG20P6)
- STARCH, CORN (UNII: O8232NY3SJ)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- TALC (UNII: 7SEV7J4R1U)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- BROWN IRON OXIDE (UNII: 1N032N7MFO)
What is the NDC to RxNorm Crosswalk for Enalapril Maleate?
- RxCUI: 858804 - enalapril maleate 2.5 MG Oral Tablet
- RxCUI: 858810 - enalapril maleate 20 MG Oral Tablet
- RxCUI: 858813 - enalapril maleate 5 MG Oral Tablet
- RxCUI: 858817 - enalapril maleate 10 MG Oral Tablet
* 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".