clonidine hydrochloride
- Product NDC
- 68382-601
- 11-digit product format
- 683820601
- Labeler code
- 68382
- Product ID
- 68382-601_2a09376a-cfc6-4134-8f2d-9e198f6d863c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- clonidine hydrochloride
- Dosage form
- INJECTION, SOLUTION
- Route
- EPIDURAL
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Application
- ANDA202601
- Marketing category
- ANDA
- Marketing start
- 2018-01-31
- Marketing end
- 0000-00-00
- Substance
- CLONIDINE HYDROCHLORIDE
- Active strength
- 0 mg/mL
- Pharmacologic classes
- Adrenergic alpha2-Agonists [MoA], Central alpha-2 Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68382-601 | CLONIDINE HYDROCHLORIDE INJECTION, SOLUTION [ZYDUS PHARMACEUTICALS USA INC.] | 4 | Legacy NDC | 20221118_f01f281d-c7e5-4258-ab14-3685f1ff296f.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68382-601-07 | 68382060107 | 1 VIAL in 1 CARTON (68382-601-07) > 10 mL in 1 VIAL | 1 vial | 2018-01-31 | 0000-00-00 | No | No | Current |