Clonidine Hydrochloride
- Product NDC
- 61442-321
- 11-digit product format
- 614420321
- Labeler code
- 61442
- Product ID
- 61442-321_1b1643e8-8b55-404d-e054-00144ff88e88
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clonidine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Carlsbad Technology, Inc
- Application
- ANDA202297
- Marketing category
- ANDA
- Marketing start
- 2013-06-17
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61442-321 | CLONIDINE HYDROCHLORIDE TABLET [CARLSBAD TECHNOLOGY, INC] | 3 | Legacy NDC | 20150717_f2c4a60b-079f-418b-8ed4-6a44de77ad51.zip |