morphine sulfate

Generic: morphine sulfate

Labeler: specgx llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name morphine sulfate
Generic Name morphine sulfate
Labeler specgx llc
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

morphine sulfate 100 mg/1

Manufacturer
SpecGx LLC

Identifiers & Regulatory

Product NDC 0406-8390
Product ID 0406-8390_6873cac9-e7d5-4db2-851d-528268b483e9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076438
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 2003-07-03

Pharmacologic Class

Classes
full opioid agonists [moa] opioid agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 04068390
Hyphenated Format 0406-8390

Supplemental Identifiers

RxCUI
891874 891881 891888 891893 892646
UPC
0304068320019
UNII
X3P646A2J0

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name morphine sulfate (source: ndc)
Generic Name morphine sulfate (source: ndc)
Application Number ANDA076438 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0406-8390-01)
  • 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0406-8390-23)
  • 100 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0406-8390-62)
source: ndc

Packages (3)

0406-8390-01 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0406-8390-01) 0406-8390-23 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0406-8390-23) 0406-8390-62 100 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0406-8390-62)

Ingredients (1)

morphine sulfate (100 mg/1)

Linked Drug Pages (1)

MORPHINE SULFATE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "6873cac9-e7d5-4db2-851d-528268b483e9", "openfda": {"upc": ["0304068320019"], "unii": ["X3P646A2J0"], "rxcui": ["891874", "891881", "891888", "891893", "892646"], "spl_set_id": ["533034fd-c8e7-495b-8874-0db41bd1e65a"], "manufacturer_name": ["SpecGx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0406-8390-01)", "package_ndc": "0406-8390-01", "marketing_start_date": "20030703"}, {"sample": false, "description": "1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0406-8390-23)", "package_ndc": "0406-8390-23", "marketing_start_date": "20030703"}, {"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0406-8390-62)", "package_ndc": "0406-8390-62", "marketing_start_date": "20030703"}], "brand_name": "MORPHINE SULFATE", "product_id": "0406-8390_6873cac9-e7d5-4db2-851d-528268b483e9", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "0406-8390", "dea_schedule": "CII", "generic_name": "MORPHINE SULFATE", "labeler_name": "SpecGx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MORPHINE SULFATE", "active_ingredients": [{"name": "MORPHINE SULFATE", "strength": "100 mg/1"}], "application_number": "ANDA076438", "marketing_category": "ANDA", "marketing_start_date": "20030703", "listing_expiration_date": "20261231"}