hydrocodone bitartrate and acetaminophen

Generic: hydrocodone bitartrate and acetaminophen

Labeler: quality care products, llc
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 quality care products, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acetaminophen 325 mg/1, hydrocodone bitartrate 10 mg/1

Manufacturer
Quality Care Products, LLC

Identifiers & Regulatory

Product NDC 55700-991
Product ID 55700-991_d63ec86d-5a5f-44ab-b335-040f0093cb64
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040400
DEA Schedule cii
Marketing Start 2022-12-27
Marketing End 2027-05-31

Pharmacologic Class

Classes
opioid agonist [epc] opioid agonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 55700991
Hyphenated Format 55700-991

Supplemental Identifiers

RxCUI
856999
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 ANDA040400 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 325 mg/1
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (55700-991-30)
  • 60 TABLET in 1 BOTTLE (55700-991-60)
  • 90 TABLET in 1 BOTTLE (55700-991-90)
source: ndc

Packages (3)

Ingredients (2)

acetaminophen (325 mg/1) hydrocodone bitartrate (10 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d63ec86d-5a5f-44ab-b335-040f0093cb64", "openfda": {"unii": ["362O9ITL9D", "NO70W886KK"], "rxcui": ["856999"], "spl_set_id": ["e7d36246-9c80-49b6-ad4b-e38c3fd6d068"], "manufacturer_name": ["Quality Care Products, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (55700-991-30)", "package_ndc": "55700-991-30", "marketing_end_date": "20270531", "marketing_start_date": "20221227"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (55700-991-60)", "package_ndc": "55700-991-60", "marketing_end_date": "20270531", "marketing_start_date": "20221227"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (55700-991-90)", "package_ndc": "55700-991-90", "marketing_end_date": "20270531", "marketing_start_date": "20221227"}], "brand_name": "HYDROCODONE BITARTRATE AND ACETAMINOPHEN", "product_id": "55700-991_d63ec86d-5a5f-44ab-b335-040f0093cb64", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "55700-991", "dea_schedule": "CII", "generic_name": "HYDROCODONE BITARTRATE AND ACETAMINOPHEN", "labeler_name": "Quality Care Products, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HYDROCODONE BITARTRATE AND ACETAMINOPHEN", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "HYDROCODONE BITARTRATE", "strength": "10 mg/1"}], "application_number": "ANDA040400", "marketing_category": "ANDA", "marketing_end_date": "20270531", "marketing_start_date": "20221227"}