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NDC 49702-0212-48 RETROVIR 10 mg/mL Details
RETROVIR 10 mg/mL
RETROVIR is a ORAL SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by ViiV Healthcare Company. The primary component is ZIDOVUDINE.
MedlinePlus Drug Summary
Zidovudine is used along with other medications to treat human immunodeficiency virus (HIV) infection. Zidovudine is given to HIV-positive pregnant women to reduce the chance of passing the infection to the baby. Zidovudine is in a class of medications called nucleoside reverse transcriptase inhibitors (NRTIs). It works by decreasing the amount of HIV in the blood. Although zidovudine does not cure HIV, it may decrease your chance of developing acquired immunodeficiency syndrome (AIDS) and HIV-related illnesses such as serious infections or cancer. Taking these medications along with practicing safer sex and making other life-style changes may decrease the risk of transmitting (spreading) the HIV virus to other people.
Related Packages: 49702-0212-48Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Zidovudine
Product Information
| NDC | 49702-0212 |
|---|---|
| Product ID | 49702-212_095c792a-11f5-4da3-b742-211876d3bc9d |
| Associated GPIs | 12108085001210 |
| GCN Sequence Number | 013023 |
| GCN Sequence Number Description | zidovudine SYRUP 10 MG/ML ORAL |
| HIC3 | W5J |
| HIC3 Description | ANTIVIRALS, HIV-SPECIFIC, NUCLEOSIDE ANALOG, RTI |
| GCN | 44410 |
| HICL Sequence Number | 004185 |
| HICL Sequence Number Description | ZIDOVUDINE |
| Brand/Generic | Brand |
| Proprietary Name | RETROVIR |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | zidovudine |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | SOLUTION |
| Route | ORAL |
| Active Ingredient Strength | 10 |
| Active Ingredient Units | mg/mL |
| Substance Name | ZIDOVUDINE |
| Labeler Name | ViiV Healthcare Company |
| Pharmaceutical Class | Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC], Nucleoside Reverse Transcriptase Inhibitors [MoA] |
| DEA Schedule | n/a |
| Marketing Category | NDA |
| Application Number | NDA019910 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 49702-0212-48 (49702021248)
| NDC Package Code | 49702-212-48 |
|---|---|
| Billing NDC | 49702021248 |
| Package | 240 mL in 1 BOTTLE (49702-212-48) |
| Marketing Start Date | 2010-10-28 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |