Clonidine Hydrochloride
- Product NDC
- 50090-2950
- 11-digit product format
- 500902950
- Labeler code
- 50090
- Product ID
- 50090-2950_0decb1e0-ccaf-449e-b235-c1567f7d6788
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clonidine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA070975
- Marketing category
- ANDA
- Marketing start
- 1995-01-03
- 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
- No
- Listing certified through
- 2019-12-31
- 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 |
|---|
| 50090-2950-0 | Clonidine Hydrochloride | 33 in 1 BOX, UNIT-DOSE | TABLET | 33 | | 10 |
| 50090-2950-0 | Clonidine Hydrochloride | 1 in 1 BLISTER PACK | TABLET | 1 | | 10 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-2950 | CLONIDINE HYDROCHLORIDE TABLET [A-S MEDICATION SOLUTIONS] | 10 | Legacy NDC, 2 package rows | 20181211_86e3f9d8-83ed-4ade-bc25-b56d8e223b8b.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50090-2950-0 | 50090295000 | 33 in 1 BOX, UNIT-DOSE | Historical |