methadone hydrochloride

Generic: methadone hydrochloride

Labeler: camber pharmaceuticals, inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methadone hydrochloride
Generic Name methadone hydrochloride
Labeler camber pharmaceuticals, inc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

methadone hydrochloride 5 mg/1

Manufacturer
Camber Pharmaceuticals, Inc

Identifiers & Regulatory

Product NDC 31722-946
Product ID 31722-946_24878a39-232d-45f6-af1f-fbb00eb5d915
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211228
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 2019-01-03

Pharmacologic Class

Classes
full opioid agonists [moa] opioid agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 31722946
Hyphenated Format 31722-946

Supplemental Identifiers

RxCUI
864706 864718
UPC
0331722947015 0331722946018
UNII
229809935B

Packaging Origin

Original Packager
true

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 methadone hydrochloride (source: ndc)
Generic Name methadone hydrochloride (source: ndc)
Application Number ANDA211228 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (31722-946-01)
source: ndc

Packages (1)

31722-946-01 100 TABLET in 1 BOTTLE (31722-946-01)

Ingredients (1)

methadone hydrochloride (5 mg/1)

Linked Drug Pages (1)

Methadone Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "24878a39-232d-45f6-af1f-fbb00eb5d915", "openfda": {"upc": ["0331722947015", "0331722946018"], "unii": ["229809935B"], "rxcui": ["864706", "864718"], "spl_set_id": ["8f4cf84e-165c-489d-a668-0f715053f196"], "manufacturer_name": ["Camber Pharmaceuticals, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (31722-946-01)", "package_ndc": "31722-946-01", "marketing_start_date": "20190103"}], "brand_name": "Methadone Hydrochloride", "product_id": "31722-946_24878a39-232d-45f6-af1f-fbb00eb5d915", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "31722-946", "dea_schedule": "CII", "generic_name": "Methadone Hydrochloride", "labeler_name": "Camber Pharmaceuticals, Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methadone Hydrochloride", "active_ingredients": [{"name": "METHADONE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA211228", "marketing_category": "ANDA", "marketing_start_date": "20190103", "listing_expiration_date": "20261231"}