Carbidopa Tablets, 25 mg
- Product NDC
- 47781-332
- 11-digit product format
- 477810332
- Labeler code
- 47781
- Product ID
- 47781-332_a397ff39-49a1-546d-8b90-6e511e2da14f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Carbidopa Tablets, 25 mg
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Alvogen Inc.
- Application
- ANDA204291
- Marketing category
- ANDA
- Marketing start
- 2016-01-25
- Marketing end
- 0000-00-00
- Substance
- CARBIDOPA
- Active strength
- 25 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 47781-332 | CARBIDOPA TABLETS, 25 MG TABLET [ALVOGEN INC.] | 12 | Legacy NDC | 20241013_97e7696c-5220-e5c3-9429-7fad5eda33fe.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 47781-332-01 | 47781033201 | 100 TABLET in 1 BOTTLE (47781-332-01) | 100 tablet | 2016-01-25 | 0000-00-00 | No | No | Current |