NDC 49884-669 Morphine Sulfate

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:
49884-669
Proprietary Name:
Morphine Sulfate
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Par Pharmaceutical Inc.
Labeler Code:
49884
Start Marketing Date: [9]
11-10-2011
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
YELLOW (C48330 - YELLOW OPAQUE CAP)
WHITE (C48325 - WHITE OPAQUE BODY)
BLUE (C48333 - BLUE VIOLET OPAQUE CAP)
BLUE (C48333 - LIGHT BLUE OPAQUE CAP)
PINK (C48328 - PINK OPAQUE CAP)
BROWN (C48332 - FLESH OPAQUE CAP)
Shape:
CAPSULE (C48336)
Size(s):
14 MM
16 MM
18 MM
19 MM
22 MM
Imprint(s):
WATSON;3449;20;MG
WATSON;3450;30;MG
WATSON;3451;50;MG
WATSON;3452;60;MG
WATSON;3576;80;MG
Score:
1

Product Details

What is NDC 49884-669?

The NDC code 49884-669 is assigned by the FDA to the product Morphine Sulfate which is product labeled by Par Pharmaceutical Inc.. The product's dosage form is . 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 Morphine Sulfate?

This medication is used to treat severe pain. Morphine belongs to a class of drugs known as opioid analgesics. It works in the brain to change how your body feels and responds to pain.

Which are Morphine Sulfate UNII Codes?

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

Which are Morphine Sulfate 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:

What is the NDC to RxNorm Crosswalk for Morphine Sulfate?

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: 892345 - morphine sulfate 30 MG Extended Release Oral Capsule
  • RxCUI: 892345 - MS 30 MG Extended Release Oral Capsule
  • RxCUI: 892352 - morphine sulfate 60 MG Extended Release Oral Capsule
  • RxCUI: 892352 - morphine sulfate 60 MG 12-24 HR Extended Release Oral Capsule
  • RxCUI: 892352 - MS 60 MG Extended Release 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".