Clonidine Hydrochloride
- Product NDC
- 68071-2699
- 11-digit product format
- 680712699
- Labeler code
- 68071
- Product ID
- 68071-2699_30b5a4cf-2c74-1eee-e063-6394a90a2b59
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clonidine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA070974
- Marketing category
- ANDA
- Marketing start
- 1995-01-03
- 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#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68071-2699-1 | Clonidine Hydrochloride | 100 in 1 BOTTLE | TABLET | 100 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68071-2699 | CLONIDINE HYDROCHLORIDE TABLET [NUCARE PHARMACEUTICALS,INC.] | 2 | Current NDC, Legacy NDC, 1 package rows | 20250322_df4b087e-a81a-1321-e053-2995a90a2b9f.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 |
|---|
| 68071-2699-1 | 68071269901 | 100 TABLET in 1 BOTTLE (68071-2699-1) | 100 tablet | 2022-05-18 | 0000-00-00 | No | No | Current |