Clonidine Hydrochloride
- Product NDC
- 71034-001
- 11-digit product format
- 710340001
- Labeler code
- 71034
- Product ID
- 71034-001_b2b1f979-6a18-ad41-e053-2995a90ad14a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clonidine Hydrochloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Xiamen LP Pharmaceutical Co., Ltd.
- Application
- ANDA209757
- Marketing category
- ANDA
- Marketing start
- 2017-12-01
- 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 | 1013930 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71034-001-60 | Clonidine Hydrochloride | 60 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 60 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71034-001 | CLONIDINE HYDROCHLORIDE TABLET, EXTENDED RELEASE [XIAMEN LP PHARMACEUTICAL CO., LTD.] | 5 | Current NDC, Legacy NDC, 1 package rows | 20201028_7676af27-4d8f-49c4-a50f-6b0892e73c8f.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71034-001-60 | 71034000160 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71034-001-60) | 2017-12-01 | 0000-00-00 | No | No | Current |