Clonidine Hydrochloride
- Product NDC
- 42291-148
- 11-digit product format
- 422910148
- Labeler code
- 42291
- Product ID
- 42291-148_d5797fc1-c8b6-5e38-e053-2995a90a8003
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clonidine Hydrochloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- AvKARE
- Application
- ANDA202984
- Marketing category
- ANDA
- Marketing start
- 2018-09-13
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 42291-148-60 | 42291014860 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (42291-148-60) | 2018-09-13 | 0000-00-00 | No | No | Current |