morphine sulfate

Generic: morphine sulfate

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name morphine sulfate
Generic Name morphine sulfate
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

morphine sulfate 30 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-9662
Product ID 71335-9662_d1b0b4ac-69d9-44bf-b7a3-229bd89b9fd6
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 713359662
Hyphenated Format 71335-9662

Supplemental Identifiers

RxCUI
892672
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
  • 30 mg/1
source: ndc
Packaging
  • 60 TABLET in 1 BOTTLE (71335-9662-1)
  • 30 TABLET in 1 BOTTLE (71335-9662-2)
  • 90 TABLET in 1 BOTTLE (71335-9662-3)
  • 120 TABLET in 1 BOTTLE (71335-9662-4)
  • 15 TABLET in 1 BOTTLE (71335-9662-5)
  • 180 TABLET in 1 BOTTLE (71335-9662-6)
  • 20 TABLET in 1 BOTTLE (71335-9662-7)
source: ndc

Packages (7)

71335-9662-1 60 TABLET in 1 BOTTLE (71335-9662-1) 71335-9662-2 30 TABLET in 1 BOTTLE (71335-9662-2) 71335-9662-3 90 TABLET in 1 BOTTLE (71335-9662-3) 71335-9662-4 120 TABLET in 1 BOTTLE (71335-9662-4) 71335-9662-5 15 TABLET in 1 BOTTLE (71335-9662-5) 71335-9662-6 180 TABLET in 1 BOTTLE (71335-9662-6) 71335-9662-7 20 TABLET in 1 BOTTLE (71335-9662-7)

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": "d1b0b4ac-69d9-44bf-b7a3-229bd89b9fd6", "openfda": {"unii": ["X3P646A2J0"], "rxcui": ["892672"], "spl_set_id": ["d1b0b4ac-69d9-44bf-b7a3-229bd89b9fd6"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-9662-1)", "package_ndc": "71335-9662-1", "marketing_start_date": "20250627"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-9662-2)", "package_ndc": "71335-9662-2", "marketing_start_date": "20250627"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-9662-3)", "package_ndc": "71335-9662-3", "marketing_start_date": "20230302"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (71335-9662-4)", "package_ndc": "71335-9662-4", "marketing_start_date": "20250627"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE (71335-9662-5)", "package_ndc": "71335-9662-5", "marketing_start_date": "20250627"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (71335-9662-6)", "package_ndc": "71335-9662-6", "marketing_start_date": "20250627"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (71335-9662-7)", "package_ndc": "71335-9662-7", "marketing_start_date": "20250627"}], "brand_name": "MORPHINE SULFATE", "product_id": "71335-9662_d1b0b4ac-69d9-44bf-b7a3-229bd89b9fd6", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "71335-9662", "dea_schedule": "CII", "generic_name": "MORPHINE SULFATE", "labeler_name": "Bryant Ranch Prepack", "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"}