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NDC 00093-9703-05 Carbidopa and levodopa 25; 250 mg/1; mg/1 Details
Carbidopa and levodopa 25; 250 mg/1; mg/1
Carbidopa and levodopa is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Teva Pharmaceuticals USA, Inc.. The primary component is CARBIDOPA; LEVODOPA.
MedlinePlus Drug Summary
The combination of levodopa and carbidopa is used to treat the symptoms of Parkinson's disease and Parkinson's-like symptoms that may develop after encephalitis (swelling of the brain) or injury to the nervous system caused by carbon monoxide poisoning or manganese poisoning. Parkinson's symptoms, including tremors (shaking), stiffness, and slowness of movement, are caused by a lack of dopamine, a natural substance usually found in the brain. Levodopa is in a class of medications called central nervous system agents. It works by being converted to dopamine in the brain. Carbidopa is in a class of medications called decarboxylase inhibitors. It works by preventing levodopa from being broken down before it reaches the brain. This allows for a lower dose of levodopa, which causes less nausea and vomiting.
Related Packages: 00093-9703-05Last Updated: 03/24/2024
MedLinePlus Full Drug Details: Levodopa and Carbidopa
Product Information
| NDC | 00093-9703 |
|---|---|
| Product ID | 0093-9703_6989f93b-c2be-4026-89b3-5cb7c4a77b73 |
| Associated GPIs | |
| GCN Sequence Number | 002539 |
| GCN Sequence Number Description | carbidopa/levodopa TABLET 25MG-250MG ORAL |
| HIC3 | H6A |
| HIC3 Description | ANTIPARKINSONISM DRUGS,OTHER |
| GCN | 62742 |
| HICL Sequence Number | 013894 |
| HICL Sequence Number Description | CARBIDOPA/LEVODOPA |
| Brand/Generic | Generic |
| Proprietary Name | Carbidopa and levodopa |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Carbidopa and levodopa |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 25; 250 |
| Active Ingredient Units | mg/1; mg/1 |
| Substance Name | CARBIDOPA; LEVODOPA |
| Labeler Name | Teva Pharmaceuticals USA, Inc. |
| Pharmaceutical Class | Amino Acids, Aromatic [CS], Aromatic Amino Acid [EPC] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA074260 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 00093-9703-05 (00093970305)
| NDC Package Code | 0093-9703-05 |
|---|---|
| Billing NDC | 00093970305 |
| Package | 500 TABLET in 1 BOTTLE (0093-9703-05) |
| Marketing Start Date | 2023-12-15 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |