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NDC 68094-0047-10 Dexmedetomidine Hydrochloride in Sodium Chloride 4 ug/mL Details
Dexmedetomidine Hydrochloride in Sodium Chloride 4 ug/mL
Dexmedetomidine Hydrochloride in Sodium Chloride is a INTRAVENOUS INJECTION, SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Precision Dose, Inc.. The primary component is DEXMEDETOMIDINE HYDROCHLORIDE.
Product Information
| NDC | 68094-0047 |
|---|---|
| Product ID | 68094-047_a72b052a-5da7-47b1-bac2-572daa7f434b |
| 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 | Dexmedetomidine Hydrochloride in Sodium Chloride |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Dexmedetomidine Hydrochloride |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | INJECTION, SOLUTION |
| Route | INTRAVENOUS |
| Active Ingredient Strength | 4 |
| Active Ingredient Units | ug/mL |
| Substance Name | DEXMEDETOMIDINE HYDROCHLORIDE |
| Labeler Name | Precision Dose, Inc. |
| Pharmaceutical Class | Adrenergic alpha2-Agonists [MoA], Central alpha-2 Adrenergic Agonist [EPC], General Anesthesia [PE] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA212857 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 68094-0047-10 (68094004710)
| NDC Package Code | 68094-047-10 |
|---|---|
| Billing NDC | 68094004710 |
| Package | 10 VIAL in 1 CARTON (68094-047-10) / 20 mL in 1 VIAL (68094-047-01) |
| Marketing Start Date | 2020-11-23 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |