Search by Drug Name or NDC
NDC 70518-3256-00 PROPOFOL 10 mg/mL Details
PROPOFOL 10 mg/mL
PROPOFOL is a INTRAVENOUS INJECTION, EMULSION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by REMEDYREPACK INC.. The primary component is PROPOFOL.
Product Information
NDC | 70518-3256 |
---|---|
Product ID | 70518-3256_f7942a59-8cb9-193f-e053-6394a90a185e |
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 | PROPOFOL |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | PROPOFOL |
Product Type | HUMAN PRESCRIPTION DRUG |
Dosage Form | INJECTION, EMULSION |
Route | INTRAVENOUS |
Active Ingredient Strength | 10 |
Active Ingredient Units | mg/mL |
Substance Name | PROPOFOL |
Labeler Name | REMEDYREPACK INC. |
Pharmaceutical Class | General Anesthesia [PE], General Anesthetic [EPC] |
DEA Schedule | n/a |
Marketing Category | ANDA |
Application Number | ANDA074848 |
Listing Certified Through | 2024-12-31 |
Package
NDC 70518-3256-00 (70518325600)
NDC Package Code | 70518-3256-0 |
---|---|
Billing NDC | 70518325600 |
Package | 10 VIAL, SINGLE-USE in 1 CARTON (70518-3256-0) / 20 mL in 1 VIAL, SINGLE-USE |
Marketing Start Date | 2021-10-25 |
NDC Exclude Flag | N |
Pricing Information | N/A |