hydrocodone bitartrate and acetaminophen

Generic: hydrocodone bitartrate and acetaminophen

Labeler: american health packaging
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 american health packaging
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

acetaminophen 325 mg/15mL, hydrocodone bitartrate 7.5 mg/15mL

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-417
Product ID 60687-417_45262987-a079-3a9e-e063-6294a90aa223
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211023
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 2019-06-19

Pharmacologic Class

Classes
opioid agonist [epc] opioid agonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60687417
Hyphenated Format 60687-417

Supplemental Identifiers

RxCUI
856940
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 ANDA211023 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 325 mg/15mL
  • 7.5 mg/15mL
source: ndc
Packaging
  • 5 TRAY in 1 CASE (60687-417-71) / 10 CUP, UNIT-DOSE in 1 TRAY (60687-417-50) / 15 mL in 1 CUP, UNIT-DOSE (60687-417-44)
source: ndc

Packages (1)

60687-417-71 5 TRAY in 1 CASE (60687-417-71) / 10 CUP, UNIT-DOSE in 1 TRAY (60687-417-50) / 15 mL in 1 CUP, UNIT-DOSE (60687-417-44)

Ingredients (2)

acetaminophen (325 mg/15mL) hydrocodone bitartrate (7.5 mg/15mL)

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": "45262987-a079-3a9e-e063-6294a90aa223", "openfda": {"unii": ["362O9ITL9D", "NO70W886KK"], "rxcui": ["856940"], "spl_set_id": ["f55d0cc9-996e-49c2-b8c1-acaceac99afe"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "5 TRAY in 1 CASE (60687-417-71)  / 10 CUP, UNIT-DOSE in 1 TRAY (60687-417-50)  / 15 mL in 1 CUP, UNIT-DOSE (60687-417-44)", "package_ndc": "60687-417-71", "marketing_start_date": "20190619"}], "brand_name": "Hydrocodone Bitartrate and Acetaminophen", "product_id": "60687-417_45262987-a079-3a9e-e063-6294a90aa223", "dosage_form": "SOLUTION", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "60687-417", "dea_schedule": "CII", "generic_name": "Hydrocodone Bitartrate and Acetaminophen", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrocodone Bitartrate and Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/15mL"}, {"name": "HYDROCODONE BITARTRATE", "strength": "7.5 mg/15mL"}], "application_number": "ANDA211023", "marketing_category": "ANDA", "marketing_start_date": "20190619", "listing_expiration_date": "20261231"}