CARBIDOPA
- Product NDC
- 70710-1221
- 11-digit product format
- 707101221
- Labeler code
- 70710
- Product ID
- 70710-1221_3abe5c9f-1e44-4fe7-b5d1-70f66f2bcfe1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CARBIDOPA
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Application
- ANDA209910
- Marketing category
- ANDA
- Marketing start
- 2018-09-06
- 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 |
|---|
| 70710-1221-1 | CARBIDOPA | 100 in 1 BOTTLE | TABLET | 100 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70710-1221 | CARBIDOPA TABLET [ZYDUS PHARMACEUTICALS USA INC.] | 5 | Current NDC, Legacy NDC, 1 package rows | 20230917_c0b1ef99-3092-431a-8fb6-897affd52595.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 |
|---|
| 70710-1221-1 | 70710122101 | 100 TABLET in 1 BOTTLE (70710-1221-1) | 100 tablet | 2018-09-06 | 0000-00-00 | No | No | Current |