Guanfacine Hydrochloride
- Product NDC
- 42291-311
- 11-digit product format
- 422910311
- Labeler code
- 42291
- Product ID
- 42291-311_78d8920c-2afc-386a-e053-2991aa0a2d73
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Guanfacine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- AvKARE, Inc.
- Application
- ANDA075109
- Marketing category
- ANDA
- Marketing start
- 2011-03-03
- Marketing end
- 0000-00-00
- Substance
- GUANFACINE HYDROCHLORIDE
- Active strength
- 2 mg/1
- Pharmacologic classes
- Central alpha-2 Adrenergic Agonist [EPC],Adrenergic alpha2-Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record