Clonidine hydrochloride
- Product NDC
- 70934-752
- 11-digit product format
- 709340752
- Labeler code
- 70934
- Product ID
- 70934-752_a9c85574-3def-738f-e053-2a95a90a17ae
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clonidine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. dba Northwind Pharmaceuticals
- Application
- ANDA070923
- Marketing category
- ANDA
- Marketing start
- 2020-05-28
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-752-60 | 70934075260 | 60 TABLET in 1 BOTTLE, PLASTIC (70934-752-60) | 60 tablet | 2020-05-28 | 0000-00-00 | No | No | Current |