NDC 64038-630 Cyclo/mag 10mg/200mg

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
64038-630
Proprietary Name:
Cyclo/mag 10mg/200mg
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
64038
Start Marketing Date: [9]
02-17-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 64038-630?

The NDC code 64038-630 is assigned by the FDA to the product Cyclo/mag 10mg/200mg which is product labeled by Living Well Pharmacy, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 64038-630-04 1 kit in 1 kit * 60 g in 1 bottle (64038-139-60) * 3 g in 1 bottle (64038-620-03). This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Cyclo/mag 10mg/200mg?

EquipmentRequired supplies needed to compound this kitEquipment ItemQuantityCyclobenzaprine HCl  (Included)3 gramsMagnesium Oxide Heavy Powder (Included)60 gramsLactose Monohydrate Spray Dried Powder ( Included)60 gramsRiboflavin Powder (Included)0.15 gramsRed 1 Capsules ( Required Not Included)300 Capsules

Which are Cyclo/mag 10mg/200mg UNII Codes?

The UNII codes for the active ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Cyclo/mag 10mg/200mg?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 999731 - cyclobenzaprine HCl 10 MG / magnesium oxide 200 MG Oral Capsule
  • RxCUI: 999731 - cyclobenzaprine hydrochloride 10 MG / magnesium oxide 200 MG Oral Capsule

* Please review the disclaimer below.

Product Footnotes

[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".