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NDC 24201-0010-50 Pentobarbital Sodium 50 mg/mL Details
Pentobarbital Sodium 50 mg/mL
Pentobarbital Sodium is a INTRAMUSCULAR; INTRAVENOUS INJECTION, SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Hikma Pharmaceuticals USA Inc. (dba Leucadia Pharmaceuticals). The primary component is PENTOBARBITAL SODIUM.
Product Information
| NDC | 24201-0010 |
|---|---|
| Product ID | 24201-010_f1ed09ca-2200-2603-e053-2995a90af46d |
| Associated GPIs | 60100055102010 |
| GCN Sequence Number | 003623 |
| GCN Sequence Number Description | pentobarbital sodium VIAL 50 MG/ML INJECTION |
| HIC3 | H2D |
| HIC3 Description | BARBITURATES |
| GCN | 13132 |
| HICL Sequence Number | 001568 |
| HICL Sequence Number Description | PENTOBARBITAL SODIUM |
| Brand/Generic | Generic |
| Proprietary Name | Pentobarbital Sodium |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Pentobarbital Sodium |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | INJECTION, SOLUTION |
| Route | INTRAMUSCULAR; INTRAVENOUS |
| Active Ingredient Strength | 50 |
| Active Ingredient Units | mg/mL |
| Substance Name | PENTOBARBITAL SODIUM |
| Labeler Name | Hikma Pharmaceuticals USA Inc. (dba Leucadia Pharmaceuticals) |
| Pharmaceutical Class | n/a |
| DEA Schedule | CII |
| Marketing Category | ANDA |
| Application Number | ANDA203619 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 24201-0010-50 (24201001050)
| NDC Package Code | 24201-010-50 |
|---|---|
| Billing NDC | 24201001050 |
| Package | 1 VIAL in 1 CARTON (24201-010-50) / 50 mL in 1 VIAL |
| Marketing Start Date | 2018-03-15 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |