Clonidine Hydrochloride
- Product NDC
- 69238-1426
- 11-digit product format
- 692381426
- Labeler code
- 69238
- Product ID
- 69238-1426_53fc2aec-b7c8-4779-96d9-03d93bd7e31c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clonidine
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Amneal Pharmaceuticals NY LLC
- Application
- ANDA210052
- Marketing category
- ANDA
- Marketing start
- 2017-11-29
- Marketing end
- 0000-00-00
- Substance
- CLONIDINE HYDROCHLORIDE
- Active strength
- 0 mg/1
- 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 |
|---|
| 69238-1426 | CLONIDINE HYDROCHLORIDE (CLONIDINE) TABLET, EXTENDED RELEASE [AMNEAL PHARMACEUTICALS NY LLC] | 14 | Legacy NDC | 20231230_accb2879-7c0e-40d9-bc78-af78fc619609.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69238-1426-6 | 69238142606 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (69238-1426-6) | 2017-11-29 | 0000-00-00 | No | No | Current |