clonidine hydrochloride
- Product NDC
- 50090-7009
- 11-digit product format
- 500907009
- Labeler code
- 50090
- Product ID
- 50090-7009_426f0c38-49b6-47b5-b26f-eadb71a801e0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- clonidine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA078895
- Marketing category
- ANDA
- Marketing start
- 2020-12-24
- Substance
- CLONIDINE HYDROCHLORIDE
- Active strength
- .1 mg/1
- Pharmacologic classes
- Adrenergic alpha2-Agonists [MoA], Central alpha-2 Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- clonidine hydrochloride
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CLONIDINE HYDROCHLORIDE | .1 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | W76I6XXF06 |
| Rxcui | 884173 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-7009-0 | clonidine hydrochloride | 50 in 1 BOX | TABLET | 50 | | 29 |
| 50090-7009-0 | clonidine hydrochloride | 1 in 1 BLISTER PACK | TABLET | 1 | | 29 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-7009 | CLONIDINE HYDROCHLORIDE TABLET [A-S MEDICATION SOLUTIONS] | 29 | Current NDC, 2 package rows | 20240110_22fbd302-46b5-4bdc-87e2-fda94cb22530.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-7009-0 | 50090700900 | 50 BLISTER PACK in 1 BOX (50090-7009-0) / 1 TABLET in 1 BLISTER PACK | 50 blister pack | 2024-01-04 | No | No | Current |