Clonidine Hydrochloride
- Product NDC
- 52584-656
- 11-digit product format
- 525840656
- Labeler code
- 52584
- Product ID
- 52584-656_bece5d23-3796-4bcc-8126-9733446f2a3c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clonidine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- General Injectables & Vaccines, Inc
- Application
- ANDA070974
- Marketing category
- ANDA
- Marketing start
- 2010-03-01
- Marketing end
- 2021-03-31
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 52584-656-61 | 52584065661 | 1 BLISTER PACK in 1 BAG (52584-656-61) > 1 TABLET in 1 BLISTER PACK | 1 blister pack | 2010-03-01 | 2021-03-31 | No | No | Current |