Anagrelide Hydrochloride
- Product NDC
- 68151-2959
- 11-digit product format
- 681512959
- Labeler code
- 68151
- Product ID
- 68151-2959_691914ba-6279-4b7c-9908-e258330fdb5b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Anagrelide Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Carilion Materials Management
- Application
- ANDA076468
- Marketing category
- ANDA
- Marketing start
- 2005-04-18
- Marketing end
- 0000-00-00
- Substance
- ANAGRELIDE HYDROCHLORIDE
- Active strength
- 1 mg/1
- Pharmacologic classes
- Decreased Platelet Production [PE],Platelet-reducing Agent [EPC],Phosphodiesterase 3 Inhibitors [MoA]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- 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 |
|---|
| 68151-2959-6 | Anagrelide Hydrochloride | 1 in 1 PACKAGE | CAPSULE | 1 | | 3 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68151-2959 | ANAGRELIDE HYDROCHLORIDE CAPSULE [CARILION MATERIALS MANAGEMENT] | 3 | Legacy NDC, 1 package rows | 20160805_614b45a3-7f2e-4348-9e20-ecf8dc440314.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 68151-2959-6 | 68151295906 | 1 in 1 PACKAGE | Historical |