Clonidine hydrochloride extended-release
- Product NDC
- 66993-776
- 11-digit product format
- 669930776
- Labeler code
- 66993
- Product ID
- 66993-776_70514816-a74b-406e-a49b-a09638399ca8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- clonidine hydrochloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Prasco Laboratories
- Application
- NDA022331
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2016-06-20
- 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 |
|---|
| 66993-776-60 | 66993077660 | 1 BOTTLE in 1 CARTON (66993-776-60) > 60 TABLET, EXTENDED RELEASE in 1 BOTTLE | 1 bottle | 2016-06-20 | 0000-00-00 | No | No | Current |