Guanfacine Hydrochloride
- Product NDC
- 50090-4119
- 11-digit product format
- 500904119
- Labeler code
- 50090
- Product ID
- 50090-4119_6ce94734-1ab4-4a40-b4f9-f4d6fe225ee1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Guanfacine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA075109
- Marketing category
- ANDA
- Marketing start
- 1998-11-25
- Marketing end
- 0000-00-00
- Substance
- GUANFACINE HYDROCHLORIDE
- Active strength
- 1 mg/1
- Pharmacologic classes
- Central alpha-2 Adrenergic Agonist [EPC],Adrenergic alpha2-Agonists [MoA]
- 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 |
|---|
| 50090-4119-0 | 50090411900 | 30 TABLET in 1 BOTTLE (50090-4119-0) | 30 tablet | 2019-02-02 | 0000-00-00 | No | No | Current |