Clonidine Hydrochloride
- Product NDC
- 50090-5105
- 11-digit product format
- 500905105
- Labeler code
- 50090
- Product ID
- 50090-5105_cff22928-9886-4751-a288-7552bc6c0e06
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Clonidine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA070974
- Marketing category
- ANDA
- Marketing start
- 1995-01-03
- 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
- 2022-12-31
- 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 |
|---|
| 50090-5105-0 | 50090510500 | 33 BLISTER PACK in 1 CARTON (50090-5105-0) > 1 TABLET in 1 BLISTER PACK | 33 blister pack | 2020-07-17 | 0000-00-00 | No | No | Current |