CLONIDINE HYDROCHLORIDE
- Product NDC
- 51662-1210
- 11-digit product format
- 516621210
- Labeler code
- 51662
- Product ID
- 51662-1210_9f0db60f-d1ea-d8dc-e053-2995a90a1be0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CLONIDINE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- HF Acquisition Co LLC, DBA HealthFirst
- Application
- ANDA070974
- Marketing category
- ANDA
- Marketing start
- 2018-11-30
- 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
- 2021-12-31
- 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 |
|---|
| 51662-1210-1 | 51662121001 | 2 BLISTER PACK in 1 BAG (51662-1210-1) > 1 TABLET in 1 BLISTER PACK | 2 blister pack | 2018-11-30 | 0000-00-00 | No | No | Current |