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buprenorphine hydrochloride
buprenorphine hydrochloride - 68308-202-30 - (buprenorphine hydrochloride)
Drug Information of buprenorphine hydrochloride
| Product NDC: | 68308-202 |
| Proprietary Name: | buprenorphine hydrochloride |
| Non Proprietary Name: | buprenorphine hydrochloride |
| Active Ingredient(s): | 2.16 mg/1 & nbsp; buprenorphine hydrochloride |
| Administration Route(s): | SUBLINGUAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of buprenorphine hydrochloride
| Product NDC: | 68308-202 |
| Labeler Name: | Midlothian Laboratories |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090622 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091101 |
Package Information of buprenorphine hydrochloride
| Package NDC: | 68308-202-30 |
| Package Description: | 30 TABLET in 1 BOTTLE (68308-202-30) |
NDC Information of buprenorphine hydrochloride
| NDC Code | 68308-202-30 |
| Proprietary Name | buprenorphine hydrochloride |
| Package Description | 30 TABLET in 1 BOTTLE (68308-202-30) |
| Product NDC | 68308-202 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | buprenorphine hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | SUBLINGUAL |
| Start Marketing Date | 20091101 |
| Marketing Category Name | ANDA |
| Labeler Name | Midlothian Laboratories |
| Substance Name | BUPRENORPHINE HYDROCHLORIDE |
| Strength Number | 2.16 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Partial Opioid Agonist [EPC],Partial Opioid Agonists [MoA] |
