Carbidopa
- Product NDC
- 68682-200
- 11-digit product format
- 686820200
- Labeler code
- 68682
- Product ID
- 68682-200_ccf10efe-4fda-40a4-8f20-1ccefb151a15
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Carbidopa Tablets
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Oceanside Pharmaceuticals
- Application
- NDA017830
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2014-04-04
- Substance
- CARBIDOPA
- Active strength
- 25 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Carbidopa
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CARBIDOPA | 25 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | MNX7R8C5VO |
| Rxcui | 260260 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68682-200-25 | Carbidopa | 100 in 1 BOTTLE | TABLET | 100 | | 8 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68682-200 | CARBIDOPA (CARBIDOPA TABLETS) TABLET [OCEANSIDE PHARMACEUTICALS] | 8 | Current NDC, Legacy NDC, 1 package rows | 20200825_d5204e5e-10ef-4758-8fc6-cb710048c687.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 |
|---|
| 68682-200-25 | 68682020025 | 100 TABLET in 1 BOTTLE (68682-200-25) | 100 tablet | 2014-04-04 | 0000-00-00 | No | No | Current |