morphine sulfate

Generic: morphine sulfate

Labeler: ascend laboratories, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name morphine sulfate
Generic Name morphine sulfate
Labeler ascend laboratories, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

morphine sulfate 30 mg/1

Manufacturer
Ascend Laboratories, LLC

Identifiers & Regulatory

Product NDC 67877-671
Product ID 67877-671_2d263950-4148-405d-b582-13857ac88044
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212451
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 2021-02-11

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 67877671
Hyphenated Format 67877-671

Supplemental Identifiers

RxCUI
892582 892672
UPC
0367877671017
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 ANDA212451 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 30 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (67877-671-01)
source: ndc

Packages (1)

67877-671-01 100 TABLET in 1 BOTTLE (67877-671-01)

Ingredients (1)

morphine sulfate (30 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": "2d263950-4148-405d-b582-13857ac88044", "openfda": {"upc": ["0367877671017"], "unii": ["X3P646A2J0"], "rxcui": ["892582", "892672"], "spl_set_id": ["07593aa4-f2c4-4d6e-b186-ab2a4ecaa38a"], "manufacturer_name": ["Ascend Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (67877-671-01)", "package_ndc": "67877-671-01", "marketing_start_date": "20210211"}], "brand_name": "MORPHINE SULFATE", "product_id": "67877-671_2d263950-4148-405d-b582-13857ac88044", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "67877-671", "dea_schedule": "CII", "generic_name": "MORPHINE SULFATE", "labeler_name": "Ascend Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MORPHINE SULFATE", "active_ingredients": [{"name": "MORPHINE SULFATE", "strength": "30 mg/1"}], "application_number": "ANDA212451", "marketing_category": "ANDA", "marketing_start_date": "20210211", "listing_expiration_date": "20261231"}