NDC 54868-0033 Dicyclomine Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-0033 - Dicyclomine Hydrochloride
Product Characteristics
Product Packages
NDC Code 54868-0033-0
Package Description: 20 CAPSULE in 1 BOTTLE, PLASTIC
NDC Code 54868-0033-2
Package Description: 100 CAPSULE in 1 BOTTLE, PLASTIC
NDC Code 54868-0033-3
Package Description: 30 CAPSULE in 1 BOTTLE, PLASTIC
NDC Code 54868-0033-5
Package Description: 40 CAPSULE in 1 BOTTLE, PLASTIC
NDC Code 54868-0033-6
Package Description: 10 CAPSULE in 1 BOTTLE, PLASTIC
NDC Code 54868-0033-7
Package Description: 60 CAPSULE in 1 BOTTLE, PLASTIC
NDC Code 54868-0033-8
Package Description: 90 CAPSULE in 1 BOTTLE, PLASTIC
Product Details
What is NDC 54868-0033?
What are the uses for Dicyclomine Hydrochloride?
Which are Dicyclomine Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- DICYCLOMINE HYDROCHLORIDE (UNII: CQ903KQA31)
- DICYCLOMINE (UNII: 4KV4X8IF6V) (Active Moiety)
Which are Dicyclomine Hydrochloride 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:
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- CALCIUM SULFATE (UNII: WAT0DDB505)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- GELATIN (UNII: 2G86QN327L)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C RED NO. 3 (UNII: PN2ZH5LOQY)
- SHELLAC (UNII: 46N107B71O)
- ALCOHOL (UNII: 3K9958V90M)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- AMMONIA (UNII: 5138Q19F1X)
- BUTYL ALCOHOL (UNII: 8PJ61P6TS3)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
What is the NDC to RxNorm Crosswalk for Dicyclomine Hydrochloride?
- RxCUI: 991061 - dicyclomine HCl 10 MG Oral Capsule
- RxCUI: 991061 - dicyclomine hydrochloride 10 MG 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".