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NDC 72865-0120-01 Methadone Hydrochloride 5 mg/1 Details
Methadone Hydrochloride 5 mg/1
Methadone Hydrochloride is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by XLCare Pharmaceuticals, Inc. The primary component is METHADONE HYDROCHLORIDE.
MedlinePlus Drug Summary
Methadone is used to relieve severe pain in people who are expected to need pain medication around the clock for a long time and who cannot be treated with other medications. It also is used to prevent withdrawal symptoms in patients who were addicted to opiate drugs and are enrolled in treatment programs in order to stop taking or continue not taking the drugs. Methadone is in a class of medications called opiate (narcotic) analgesics. Methadone works to treat pain by changing the way the brain and nervous system respond to pain. It works to treat people who were addicted to opiate drugs by producing similar effects and preventing withdrawal symptoms in people who have stopped using these drugs.
Related Packages: 72865-0120-01Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Methadone
Product Information
| NDC | 72865-0120 |
|---|---|
| Product ID | 72865-120_ecea9406-f092-4953-93e8-92b3c26a57bf |
| Associated GPIs | 65100050100305 |
| GCN Sequence Number | 004242 |
| GCN Sequence Number Description | methadone HCl TABLET 5 MG ORAL |
| HIC3 | H3A |
| HIC3 Description | OPIOID ANALGESICS |
| GCN | 16422 |
| HICL Sequence Number | 001745 |
| HICL Sequence Number Description | METHADONE HCL |
| Brand/Generic | Generic |
| Proprietary Name | Methadone Hydrochloride |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Methadone Hydrochloride |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 5 |
| Active Ingredient Units | mg/1 |
| Substance Name | METHADONE HYDROCHLORIDE |
| Labeler Name | XLCare Pharmaceuticals, Inc |
| Pharmaceutical Class | Full Opioid Agonists [MoA], Opioid Agonist [EPC] |
| DEA Schedule | CII |
| Marketing Category | ANDA |
| Application Number | ANDA211228 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 72865-0120-01 (72865012001)
| NDC Package Code | 72865-120-01 |
|---|---|
| Billing NDC | 72865012001 |
| Package | 100 TABLET in 1 BOTTLE (72865-120-01) |
| Marketing Start Date | 2019-01-03 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |