Clonidine Hydrochloride
- Product NDC
- 64725-2957
- 11-digit product format
- 647252957
- Labeler code
- 64725
- Product ID
- 64725-2957_26fe7a22-53d6-4b55-b20f-d88c0f7f75b6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- clonidine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- TYA Pharmaceuticals
- Application
- ANDA077901
- Marketing category
- ANDA
- Marketing start
- 2007-03-09
- Marketing end
- 0000-00-00
- Substance
- CLONIDINE HYDROCHLORIDE
- Active strength
- 0 mg/1
- Pharmacologic classes
- Adrenergic alpha2-Agonists [MoA],Central alpha-2 Adrenergic Agonist [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 64725-2957-1 | Clonidine Hydrochloride | 100 in 1 BOTTLE | TABLET | 100 | | 2 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 64725-2957 | CLONIDINE HYDROCHLORIDE TABLET [TYA PHARMACEUTICALS] | 2 | Legacy NDC, 1 package rows | 20140901_e4e47a73-c29d-43b3-8998-d08e44ada73e.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 64725-2957-1 | 64725295701 | 100 in 1 BOTTLE | Historical |