Guanfacine Hydrochloride
- Product NDC
- 0378-1061
- 11-digit product format
- 003781061
- Labeler code
- 0378
- Product ID
- 0378-1061_9c685c1b-b62c-4bc9-b105-609fb0df7ef6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- guanfacine
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Mylan Pharmaceuticals Inc.
- Application
- ANDA202578
- Marketing category
- ANDA
- Marketing start
- 2015-06-02
- Marketing end
- 2019-11-30
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record