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NDC 70518-2217-00 BUPRENORPHINE 2 mg/1 Details
BUPRENORPHINE 2 mg/1
BUPRENORPHINE is a SUBLINGUAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by REMEDYREPACK INC.. The primary component is BUPRENORPHINE HYDROCHLORIDE.
Product Information
| NDC | 70518-2217 |
|---|---|
| Product ID | 70518-2217_03859559-a744-09c5-e063-6294a90ab890 |
| Associated GPIs | |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | BUPRENORPHINE |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | BUPRENORPHINE |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET |
| Route | SUBLINGUAL |
| Active Ingredient Strength | 2 |
| Active Ingredient Units | mg/1 |
| Substance Name | BUPRENORPHINE HYDROCHLORIDE |
| Labeler Name | REMEDYREPACK INC. |
| Pharmaceutical Class | Partial Opioid Agonist [EPC], Partial Opioid Agonists [MoA] |
| DEA Schedule | CIII |
| Marketing Category | ANDA |
| Application Number | ANDA207276 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 70518-2217-00 (70518221700)
| NDC Package Code | 70518-2217-0 |
|---|---|
| Billing NDC | 70518221700 |
| Package | 30 TABLET in 1 BLISTER PACK (70518-2217-0) |
| Marketing Start Date | 2019-07-15 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |