hydrocodone bitartrate and acetaminophen

Generic: hydrocodone bitartrate and acetaminophen

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

Drug Facts

Product Profile

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

acetaminophen 325 mg/1, hydrocodone bitartrate 5 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 63187-112
Product ID 63187-112_160e7aae-4a67-4845-9fa1-9d13afb5285d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040736
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 2010-01-18

Pharmacologic Class

Classes
opioid agonist [epc] opioid agonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63187112
Hyphenated Format 63187-112

Supplemental Identifiers

RxCUI
857002
UNII
362O9ITL9D NO70W886KK

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 hydrocodone bitartrate and acetaminophen (source: ndc)
Generic Name hydrocodone bitartrate and acetaminophen (source: ndc)
Application Number ANDA040736 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 325 mg/1
  • 5 mg/1
source: ndc
Packaging
  • 15 TABLET in 1 BOTTLE (63187-112-15)
  • 20 TABLET in 1 BOTTLE (63187-112-20)
  • 30 TABLET in 1 BOTTLE (63187-112-30)
  • 60 TABLET in 1 BOTTLE (63187-112-60)
source: ndc

Packages (4)

63187-112-15 15 TABLET in 1 BOTTLE (63187-112-15) 63187-112-20 20 TABLET in 1 BOTTLE (63187-112-20) 63187-112-30 30 TABLET in 1 BOTTLE (63187-112-30) 63187-112-60 60 TABLET in 1 BOTTLE (63187-112-60)

Ingredients (2)

acetaminophen (325 mg/1) hydrocodone bitartrate (5 mg/1)

Linked Drug Pages (1)

Hydrocodone Bitartrate and Acetaminophen ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "160e7aae-4a67-4845-9fa1-9d13afb5285d", "openfda": {"unii": ["362O9ITL9D", "NO70W886KK"], "rxcui": ["857002"], "spl_set_id": ["50be5d00-758e-4d01-8e78-40a60dbe67e5"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET in 1 BOTTLE (63187-112-15)", "package_ndc": "63187-112-15", "marketing_start_date": "20140602"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (63187-112-20)", "package_ndc": "63187-112-20", "marketing_start_date": "20140602"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (63187-112-30)", "package_ndc": "63187-112-30", "marketing_start_date": "20140602"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (63187-112-60)", "package_ndc": "63187-112-60", "marketing_start_date": "20140602"}], "brand_name": "Hydrocodone Bitartrate and Acetaminophen", "product_id": "63187-112_160e7aae-4a67-4845-9fa1-9d13afb5285d", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "63187-112", "dea_schedule": "CII", "generic_name": "Hydrocodone Bitartrate and Acetaminophen", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrocodone Bitartrate and Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "HYDROCODONE BITARTRATE", "strength": "5 mg/1"}], "application_number": "ANDA040736", "marketing_category": "ANDA", "marketing_start_date": "20100118", "listing_expiration_date": "20261231"}