clonidine hydrochloride
- Product NDC
- 51655-339
- 11-digit product format
- 516550339
- Labeler code
- 51655
- Product ID
- 51655-339_48eb2827-d0cc-684b-e063-6294a90a8388
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- clonidine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Northwind Health Company, LLC
- Application
- ANDA078895
- Marketing category
- ANDA
- Marketing start
- 2020-05-27
- 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
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- clonidine hydrochloride
- Listing expiration
- 2027-12-31
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#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51655-339-25 | clonidine hydrochloride | 60 in 1 BOTTLE, PLASTIC | TABLET | 60 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51655-339 | CLONIDINE HYDROCHLORIDE TABLET [NORTHWIND PHARMACEUTICALS, LLC] | 3 | Current NDC, Legacy NDC, 1 package rows | 20231115_ab2ffb6e-7070-063b-e053-2a95a90aff22.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 |
|---|
| 51655-339-25 | 51655033925 | 60 TABLET in 1 BOTTLE, PLASTIC (51655-339-25) | 60 tablet | 2020-05-27 | 0000-00-00 | No | No | Current |