NDC 43353-688 Premarin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43353 - Aphena Pharma Solutions - Tennessee, Inc.
- 43353-688 - Premarin
Product Characteristics
Product Packages
NDC Code 43353-688-60
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Product Details
What is NDC 43353-688?
What are the uses for Premarin?
Which are Premarin UNII Codes?
The UNII codes for the active ingredients in this product are:
- ESTROGENS, CONJUGATED (UNII: IU5QR144QX)
- ESTROGENS, CONJUGATED (UNII: IU5QR144QX) (Active Moiety)
Which are Premarin 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:
- TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)
- HYDROXYPROPYL CELLULOSE (UNII: RFW2ET671P)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POWDERED CELLULOSE (UNII: SMD1X3XO9M)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- SUCROSE (UNII: C151H8M554)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- HYPROMELLOSE 2208 (15000 MPA.S) (UNII: Z78RG6M2N2)
- HYPROMELLOSE 2910 (6 MPA.S) (UNII: 0WZ8WG20P6)
- HYPROMELLOSE 2910 (15 MPA.S) (UNII: 36SFW2JZ0W)
What is the NDC to RxNorm Crosswalk for Premarin?
- RxCUI: 150840 - PREMARIN 0.625 MG Oral Tablet
- RxCUI: 150840 - estrogens, conjugated (USP) 0.625 MG Oral Tablet [Premarin]
- RxCUI: 150840 - Premarin 0.625 MG Oral Tablet
- RxCUI: 197660 - estrogens, conjugated 0.3 MG Oral Tablet
- RxCUI: 197660 - estrogens, conjugated (USP) 0.3 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".