Clonidine Hydrochloride
- Product NDC
- 63629-2317
- 11-digit product format
- 636292317
- Labeler code
- 63629
- Product ID
- 63629-2317_42c16461-8edf-4983-995d-fc856a4942dd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clonidine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA202297
- Marketing category
- ANDA
- Marketing start
- 2020-07-01
- Substance
- CLONIDINE HYDROCHLORIDE
- Active strength
- .2 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 | .2 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | W76I6XXF06 |
| Rxcui | 884185 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 63629-2317-1 | Clonidine Hydrochloride | 100 in 1 BOTTLE | TABLET | 100 | | 107 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63629-2317 | CLONIDINE HYDROCHLORIDE TABLET [BRYANT RANCH PREPACK] | 107 | Current NDC, Legacy NDC, 1 package rows | 20250323_74b40ae9-a9d7-443e-8d7a-80362ec5be6d.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-2317-1 | 63629231701 | 100 TABLET in 1 BOTTLE (63629-2317-1) | 100 tablet | 2020-07-01 | 0000-00-00 | No | No | Current |