Clonidine hydrochloride
- Product NDC
- 71610-449
- 11-digit product format
- 716100449
- Labeler code
- 71610
- Product ID
- 71610-449_6e5cec35-31fa-4db7-a681-cd264ebd6cbf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clonidine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA070923
- Marketing category
- ANDA
- Marketing start
- 2017-06-01
- Substance
- CLONIDINE HYDROCHLORIDE
- Active strength
- .3 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 | .3 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | W76I6XXF06 |
| Rxcui | 884189 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71610-449-09 | Clonidine hydrochloride | 9000 in 1 BOTTLE | TABLET | 9000 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71610-449 | CLONIDINE HYDROCHLORIDE TABLET [APHENA PHARMA SOLUTIONS - TENNESSEE, LLC] | 1 | Current NDC, Legacy NDC, 1 package rows | 20200731_00d1562d-b4eb-4d89-95de-0aacee7a82a5.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 |
|---|
| 71610-449-09 | 71610044909 | 9000 TABLET in 1 BOTTLE (71610-449-09) | 9000 tablet | 2020-07-28 | 0000-00-00 | No | No | Current |