buprenorphine hydrochloride and naloxone hydrochloride dihydrate

Generic: buprenorphine hydrochloride and naloxone hydrochloride dihydrate

Labeler: redpharm drug
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name buprenorphine hydrochloride and naloxone hydrochloride dihydrate
Generic Name buprenorphine hydrochloride and naloxone hydrochloride dihydrate
Labeler redpharm drug
Dosage Form TABLET
Routes
SUBLINGUAL
Active Ingredients

buprenorphine hydrochloride 8 mg/1, naloxone hydrochloride dihydrate 2 mg/1

Manufacturer
Redpharm Drug

Identifiers & Regulatory

Product NDC 67296-2191
Product ID 67296-2191_490df063-a9d0-7d96-e063-6394a90a1e15
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209069
DEA Schedule ciii
Listing Expiration 2027-12-31
Marketing Start 2020-09-01

Pharmacologic Class

Classes
opioid antagonist [epc] opioid antagonists [moa] partial opioid agonist [epc] partial opioid agonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 672962191
Hyphenated Format 67296-2191

Supplemental Identifiers

RxCUI
351267
UPC
0316729550109 0316729549103
UNII
56W8MW3EN1 5Q187997EE

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 buprenorphine hydrochloride and naloxone hydrochloride dihydrate (source: ndc)
Generic Name buprenorphine hydrochloride and naloxone hydrochloride dihydrate (source: ndc)
Application Number ANDA209069 (source: ndc)
Routes
SUBLINGUAL
source: ndc

Resolved Composition

Strengths
  • 8 mg/1
  • 2 mg/1
source: ndc
Packaging
  • 12 TABLET in 1 BOTTLE, PLASTIC (67296-2191-1)
  • 6 TABLET in 1 BOTTLE, PLASTIC (67296-2191-6)
source: ndc

Packages (2)

67296-2191-1 12 TABLET in 1 BOTTLE, PLASTIC (67296-2191-1) 67296-2191-6 6 TABLET in 1 BOTTLE, PLASTIC (67296-2191-6)

Ingredients (2)

buprenorphine hydrochloride (8 mg/1) naloxone hydrochloride dihydrate (2 mg/1)

Linked Drug Pages (1)

BUPRENORPHINE HYDROCHLORIDE and NALOXONE HYDROCHLORIDE DIHYDRATE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["SUBLINGUAL"], "spl_id": "490df063-a9d0-7d96-e063-6394a90a1e15", "openfda": {"upc": ["0316729550109", "0316729549103"], "unii": ["56W8MW3EN1", "5Q187997EE"], "rxcui": ["351267"], "spl_set_id": ["44f2e26f-4586-5204-e063-6394a90a47d5"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "12 TABLET in 1 BOTTLE, PLASTIC (67296-2191-1)", "package_ndc": "67296-2191-1", "marketing_start_date": "20200901"}, {"sample": false, "description": "6 TABLET in 1 BOTTLE, PLASTIC (67296-2191-6)", "package_ndc": "67296-2191-6", "marketing_start_date": "20200901"}], "brand_name": "BUPRENORPHINE HYDROCHLORIDE and NALOXONE HYDROCHLORIDE DIHYDRATE", "product_id": "67296-2191_490df063-a9d0-7d96-e063-6394a90a1e15", "dosage_form": "TABLET", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]", "Partial Opioid Agonist [EPC]", "Partial Opioid Agonists [MoA]"], "product_ndc": "67296-2191", "dea_schedule": "CIII", "generic_name": "BUPRENORPHINE HYDROCHLORIDE and NALOXONE HYDROCHLORIDE DIHYDRATE", "labeler_name": "Redpharm Drug", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "BUPRENORPHINE HYDROCHLORIDE and NALOXONE HYDROCHLORIDE DIHYDRATE", "active_ingredients": [{"name": "BUPRENORPHINE HYDROCHLORIDE", "strength": "8 mg/1"}, {"name": "NALOXONE HYDROCHLORIDE DIHYDRATE", "strength": "2 mg/1"}], "application_number": "ANDA209069", "marketing_category": "ANDA", "marketing_start_date": "20200901", "listing_expiration_date": "20271231"}