morphine sulfate

Generic: morphine sulfate

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name morphine sulfate
Generic Name morphine sulfate
Labeler american health packaging
Dosage Form TABLET
Routes
ORAL
Active Ingredients

morphine sulfate 15 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-617
Product ID 60687-617_45364b66-8b1b-f778-e063-6394a90aa2e1
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212451
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 2021-10-18

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60687617
Hyphenated Format 60687-617

Supplemental Identifiers

RxCUI
892582
UNII
X3P646A2J0

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
  • 15 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-617-01) / 1 TABLET in 1 BLISTER PACK (60687-617-11)
source: ndc

Packages (1)

Ingredients (1)

morphine sulfate (15 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "45364b66-8b1b-f778-e063-6394a90aa2e1", "openfda": {"unii": ["X3P646A2J0"], "rxcui": ["892582"], "spl_set_id": ["d66d0cfb-9bfe-490c-90ee-49481c567e85"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-617-01)  / 1 TABLET in 1 BLISTER PACK (60687-617-11)", "package_ndc": "60687-617-01", "marketing_start_date": "20211018"}], "brand_name": "Morphine Sulfate", "product_id": "60687-617_45364b66-8b1b-f778-e063-6394a90aa2e1", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "60687-617", "dea_schedule": "CII", "generic_name": "Morphine Sulfate", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Morphine Sulfate", "active_ingredients": [{"name": "MORPHINE SULFATE", "strength": "15 mg/1"}], "application_number": "ANDA212451", "marketing_category": "ANDA", "marketing_start_date": "20211018", "listing_expiration_date": "20261231"}