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NDC 43598-0579-30 Buprenorphine and Naloxone 2; .5 mg/1; mg/1 Details
Buprenorphine and Naloxone 2; .5 mg/1; mg/1
Buprenorphine and Naloxone is a BUCCAL; SUBLINGUAL FILM, SOLUBLE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Dr.Reddys Laboratories Inc. The primary component is BUPRENORPHINE HYDROCHLORIDE; NALOXONE.
MedlinePlus Drug Summary
Buprenorphine and the combination of buprenorphine and naloxone are used to treat opioid dependence (addiction to opioid drugs, including heroin and narcotic painkillers). Buprenorphine is in a class of medications called opioid partial agonist-antagonists and naloxone is in a class of medications called opioid antagonists. Buprenorphine alone and the combination of buprenorphine and naloxone work to prevent withdrawal symptoms when someone stops taking opioid drugs by producing similar effects to these drugs.
Related Packages: 43598-0579-30Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Buprenorphine Sublingual and Buccal (opioid dependence)
Product Information
| NDC | 43598-0579 |
|---|---|
| Product ID | 43598-579_06eedb87-f2e6-d9f9-c23c-7b2c975239c7 |
| Associated GPIs | 65200010208220 |
| GCN Sequence Number | 066635 |
| GCN Sequence Number Description | buprenorphine HCl/naloxone HCl FILM 2 MG-0.5MG SUBLINGUAL |
| HIC3 | H3W |
| HIC3 Description | OPIOID WITHDRAWAL THERAPY AGENTS, OPIOID-TYPE |
| GCN | 28958 |
| HICL Sequence Number | 024846 |
| HICL Sequence Number Description | BUPRENORPHINE HCL/NALOXONE HCL |
| Brand/Generic | Generic |
| Proprietary Name | Buprenorphine and Naloxone |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Buprenorphine and Naloxone |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | FILM, SOLUBLE |
| Route | BUCCAL; SUBLINGUAL |
| Active Ingredient Strength | 2; .5 |
| Active Ingredient Units | mg/1; mg/1 |
| Substance Name | BUPRENORPHINE HYDROCHLORIDE; NALOXONE |
| Labeler Name | Dr.Reddys Laboratories Inc |
| Pharmaceutical Class | Opioid Antagonist [EPC], Opioid Antagonists [MoA], Partial Opioid Agonist [EPC], Partial Opioid Agonists [MoA] |
| DEA Schedule | CIII |
| Marketing Category | ANDA |
| Application Number | ANDA205299 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 43598-0579-30 (43598057930)
| NDC Package Code | 43598-579-30 |
|---|---|
| Billing NDC | 43598057930 |
| Package | 30 POUCH in 1 CARTON (43598-579-30) / 1 FILM, SOLUBLE in 1 POUCH (43598-579-01) |
| Marketing Start Date | 2018-06-14 |
| NDC Exclude Flag | N |
| Pricing Information | |
| Price Per Unit | 2.06222 |
| Pricing Unit | EA |
| Effective Date | 2024-02-21 |
| NDC Description | BUPRENORPHINE-NALOXONE 2-0.5 MG SL FILM |
| Pharmacy Type Indicator | C/I |
| OTC | N |
| Explanation Code | 1 |
| Classification for Rate Setting | G |
| As of Date | 2024-02-21 |
This pricing file, entitled the NADAC (National Average Drug Acquisition
Cost) files, provide
state Medicaid agencies with covered outpatient drug prices by averaging
survey invoice
prices from retail community pharmacies across the United States. These
pharmacies include
independent retail community pharmacies and chain pharmacies. The prices
are updated on a
weekly and monthly basis