hydrocodone bitartrate and acetaminophen

Generic: hydrocodone bitartrate and acetaminophen

Labeler: Eywa Pharma Inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Active

Drug Facts

Product Profile

Brand Name hydrocodone bitartrate and acetaminophen
Generic Name hydrocodone bitartrate and acetaminophen
Labeler Eywa Pharma Inc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

ACETAMINOPHEN 300 mg/1, HYDROCODONE BITARTRATE 10 mg/1

Identifiers & Regulatory

Product NDC 71930-044
Product ID 71930-044_e620604d-aacd-41bd-a5e7-c380badc000f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207509
DEA Schedule CII
Listing Expiration 2027-12-31
Marketing Start 2019-06-17

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71930044
Hyphenated Format 71930-044

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 ANDA207509 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 300 mg/1
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (71930-044-12)
  • 500 TABLET in 1 BOTTLE (71930-044-52)
source: ndc

Packages (2)

71930-044-12 100 TABLET in 1 BOTTLE (71930-044-12) 71930-044-52 500 TABLET in 1 BOTTLE (71930-044-52)

Ingredients (2)

ACETAMINOPHEN (300 mg/1) HYDROCODONE BITARTRATE (10 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": "e620604d-aacd-41bd-a5e7-c380badc000f", "openfda": {"upc": ["0371930044120"], "unii": ["362O9ITL9D", "NO70W886KK"], "rxcui": ["856980", "856987", "856992"], "spl_set_id": ["8a201e19-3e47-7e58-e053-2995a90ab1d5"], "manufacturer_name": ["Eywa Pharma Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (71930-044-12)", "package_ndc": "71930-044-12", "marketing_start_date": "20190617"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (71930-044-52)", "package_ndc": "71930-044-52", "marketing_start_date": "20190617"}], "brand_name": "hydrocodone bitartrate and acetaminophen", "product_id": "71930-044_e620604d-aacd-41bd-a5e7-c380badc000f", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "71930-044", "dea_schedule": "CII", "generic_name": "hydrocodone bitartrate and acetaminophen", "labeler_name": "Eywa Pharma Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "hydrocodone bitartrate and acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "300 mg/1"}, {"name": "HYDROCODONE BITARTRATE", "strength": "10 mg/1"}], "application_number": "ANDA207509", "marketing_category": "ANDA", "marketing_start_date": "20190617", "listing_expiration_date": "20271231"}