NDC 68645-230 Belladonna Alkaloids With Phenobartbital
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 68645-230?
What are the uses for Belladonna Alkaloids With Phenobartbital?
Which are Belladonna Alkaloids With Phenobartbital UNII Codes?
The UNII codes for the active ingredients in this product are:
- ATROPINE SULFATE (UNII: 03J5ZE7KA5)
- ATROPINE (UNII: 7C0697DR9I) (Active Moiety)
- HYOSCYAMINE SULFATE (UNII: F2R8V82B84)
- HYOSCYAMINE (UNII: PX44XO846X) (Active Moiety)
- SCOPOLAMINE HYDROBROMIDE (UNII: 451IFR0GXB)
- SCOPOLAMINE (UNII: DL48G20X8X) (Active Moiety)
- PHENOBARBITAL (UNII: YQE403BP4D)
- PHENOBARBITAL (UNII: YQE403BP4D) (Active Moiety)
Which are Belladonna Alkaloids With Phenobartbital 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)
- CALCIUM STEARATE (UNII: 776XM7047L)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- STARCH, CORN (UNII: O8232NY3SJ)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
What is the NDC to RxNorm Crosswalk for Belladonna Alkaloids With Phenobartbital?
- RxCUI: 1046815 - atropine sulfate 0.0194 MG / hyoscyamine sulfate 0.1037 MG / PHENobarbital 16.2 MG / scopolamine HBr 0.0065 MG Oral Tablet
- RxCUI: 1046815 - atropine sulfate 0.0194 MG / hyoscyamine sulfate 0.1037 MG / phenobarbital 16.2 MG / scopolamine hydrobromide 0.0065 MG Oral Tablet
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
[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".