Clonidine Hydrochloride
- Product NDC
- 67046-327
- 11-digit product format
- 670460327
- Labeler code
- 67046
- Product ID
- 67046-327_bcce62a6-7ceb-a058-e053-2995a90a558c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clonidine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Contract Pharmacy Services-PA
- Application
- ANDA070975
- Marketing category
- ANDA
- Marketing start
- 2020-01-09
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 67046-327-30 | 67046032730 | 30 TABLET in 1 BLISTER PACK (67046-327-30) | 30 tablet | 2020-01-09 | 0000-00-00 | No | No | Current |