Carbidopa and Levodopa
- Product NDC
- 63739-107
- 11-digit product format
- 637390107
- Labeler code
- 63739
- Product ID
- 63739-107_b959e504-eec5-f0d9-e053-2995a90ab6f0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Carbidopa and Levodopa
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- McKesson Corporation dba SKY Packaging
- Application
- ANDA073618
- Marketing category
- ANDA
- Marketing start
- 2018-07-16
- Marketing end
- 0000-00-00
- Substance
- CARBIDOPA; LEVODOPA
- Active strength
- 10 mg/1; mg/1
- Pharmacologic classes
- Aromatic Amino Acid [EPC],Amino Acids, Aromatic [CS]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 63739-107-10 | Carbidopa and Levodopa | 10 in 1 BLISTER PACK | TABLET | 10 | | 10 |
| 63739-107-10 | Carbidopa and Levodopa | 10 in 1 BOX | TABLET | 10 | | 10 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63739-107 | CARBIDOPA AND LEVODOPA TABLET [MCKESSON CORPORATION DBA SKY PACKAGING] | 10 | Legacy NDC, 2 package rows | 20210121_180c0ec8-6314-4681-8b69-a5d612c5c927.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63739-107-10 | 63739010710 | 10 BLISTER PACK in 1 BOX (63739-107-10) > 10 TABLET in 1 BLISTER PACK | 10 blister pack | 2019-04-15 | 2021-08-31 | No | No | Current |