NDC 21695-033 Clindamycin Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 21695 - Rebel Distributors Corp
- 21695-033 - Clindamycin Hydrochloride
Product Characteristics
GREEN (C48329 - LIGHT GREEN)
Product Packages
NDC Code 21695-033-12
Package Description: 12 CAPSULE in 1 BOTTLE
NDC Code 21695-033-21
Package Description: 21 CAPSULE in 1 BOTTLE
NDC Code 21695-033-28
Package Description: 28 CAPSULE in 1 BOTTLE
NDC Code 21695-033-40
Package Description: 40 CAPSULE in 1 BOTTLE
NDC Code 21695-033-60
Package Description: 60 CAPSULE in 1 BOTTLE
NDC Code 21695-033-90
Package Description: 90 CAPSULE in 1 BOTTLE
Product Details
What is NDC 21695-033?
What are the uses for Clindamycin Hydrochloride?
Which are Clindamycin Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- CLINDAMYCIN HYDROCHLORIDE (UNII: T20OQ1YN1W)
- CLINDAMYCIN (UNII: 3U02EL437C) (Active Moiety)
Which are Clindamycin 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:
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- STARCH, CORN (UNII: O8232NY3SJ)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- GELATIN (UNII: 2G86QN327L)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Clindamycin Hydrochloride?
- RxCUI: 197518 - clindamycin HCl 150 MG Oral Capsule
- RxCUI: 197518 - clindamycin 150 MG Oral Capsule
- RxCUI: 197518 - clindamycin (as clindamycin HCl) 150 MG Oral Capsule
- RxCUI: 284215 - clindamycin HCl 300 MG Oral Capsule
- RxCUI: 284215 - clindamycin 300 MG Oral Capsule
* 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".