NDC 47335-927 Aspirin And Dipyridamole Extended Release
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 47335 - Sun Pharmaceutical Industries, Inc.
- 47335-927 - Aspirin And Dipyridamole Extended Release
Product Characteristics
WHITE (C48325 - IVORY)
Product Packages
NDC Code 47335-927-83
Package Description: 30 CAPSULE in 1 BOTTLE
NDC Code 47335-927-86
Package Description: 60 CAPSULE in 1 BOTTLE
Product Details
What is NDC 47335-927?
What are the uses for Aspirin And Dipyridamole Extended Release?
Which are Aspirin And Dipyridamole Extended Release UNII Codes?
The UNII codes for the active ingredients in this product are:
- ASPIRIN (UNII: R16CO5Y76E)
- ASPIRIN (UNII: R16CO5Y76E) (Active Moiety)
- DIPYRIDAMOLE (UNII: 64ALC7F90C)
- DIPYRIDAMOLE (UNII: 64ALC7F90C) (Active Moiety)
Which are Aspirin And Dipyridamole Extended 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:
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- GELATIN (UNII: 2G86QN327L)
- WATER (UNII: 059QF0KO0R)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SHELLAC (UNII: 46N107B71O)
- ALCOHOL (UNII: 3K9958V90M)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- BUTYL ALCOHOL (UNII: 8PJ61P6TS3)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- AMMONIA (UNII: 5138Q19F1X)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
- TARTARIC ACID (UNII: W4888I119H)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- ACACIA (UNII: 5C5403N26O)
- TALC (UNII: 7SEV7J4R1U)
- METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:2) (UNII: 5KY68S2577)
- HYPROMELLOSE PHTHALATE (31% PHTHALATE, 40 CST) (UNII: G4U024CQK6)
- TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
- STARCH, CORN (UNII: O8232NY3SJ)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- TRIACETIN (UNII: XHX3C3X673)
- ETHYLCELLULOSES (UNII: 7Z8S9VYZ4B)
What is the NDC to RxNorm Crosswalk for Aspirin And Dipyridamole Extended Release?
- RxCUI: 259081 - aspirin 25 MG / dipyridamole 200 MG 12HR Extended Release Oral Capsule
- RxCUI: 259081 - 12 HR aspirin 25 MG / dipyridamole 200 MG Extended Release Oral Capsule
- RxCUI: 259081 - 12 HR ASA 25 MG / Dipyridamole 200 MG Extended Release Oral Capsule
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[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".