acetaminophen and codeine phosphate

Generic: acetaminophen and codeine phosphate

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name acetaminophen and codeine phosphate
Generic Name acetaminophen and codeine phosphate
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acetaminophen 300 mg/1, codeine phosphate 30 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 63187-815
Product ID 63187-815_5dde8fb0-3744-4a96-89c4-5b891681ccd9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202800
DEA Schedule ciii
Listing Expiration 2026-12-31
Marketing Start 2017-01-05

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63187815
Hyphenated Format 63187-815

Supplemental Identifiers

RxCUI
993781
UPC
0363187815158
UNII
362O9ITL9D GSL05Y1MN6

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 acetaminophen and codeine phosphate (source: ndc)
Generic Name acetaminophen and codeine phosphate (source: ndc)
Application Number ANDA202800 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 300 mg/1
  • 30 mg/1
source: ndc
Packaging
  • 15 TABLET in 1 BOTTLE (63187-815-15)
  • 20 TABLET in 1 BOTTLE (63187-815-20)
  • 30 TABLET in 1 BOTTLE (63187-815-30)
  • 60 TABLET in 1 BOTTLE (63187-815-60)
source: ndc

Packages (4)

63187-815-15 15 TABLET in 1 BOTTLE (63187-815-15) 63187-815-20 20 TABLET in 1 BOTTLE (63187-815-20) 63187-815-30 30 TABLET in 1 BOTTLE (63187-815-30) 63187-815-60 60 TABLET in 1 BOTTLE (63187-815-60)

Ingredients (2)

acetaminophen (300 mg/1) codeine phosphate (30 mg/1)

Linked Drug Pages (1)

Acetaminophen and Codeine Phosphate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "5dde8fb0-3744-4a96-89c4-5b891681ccd9", "openfda": {"upc": ["0363187815158"], "unii": ["362O9ITL9D", "GSL05Y1MN6"], "rxcui": ["993781"], "spl_set_id": ["75b50751-5237-4e3e-b7ee-1605c0602f3b"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET in 1 BOTTLE (63187-815-15)", "package_ndc": "63187-815-15", "marketing_start_date": "20200528"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (63187-815-20)", "package_ndc": "63187-815-20", "marketing_start_date": "20170201"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (63187-815-30)", "package_ndc": "63187-815-30", "marketing_start_date": "20170201"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (63187-815-60)", "package_ndc": "63187-815-60", "marketing_start_date": "20170201"}], "brand_name": "Acetaminophen and Codeine Phosphate", "product_id": "63187-815_5dde8fb0-3744-4a96-89c4-5b891681ccd9", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "63187-815", "dea_schedule": "CIII", "generic_name": "Acetaminophen and Codeine Phosphate", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Acetaminophen and Codeine Phosphate", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "300 mg/1"}, {"name": "CODEINE PHOSPHATE", "strength": "30 mg/1"}], "application_number": "ANDA202800", "marketing_category": "ANDA", "marketing_start_date": "20170105", "listing_expiration_date": "20261231"}