Guanfacine
- Product NDC
- 0781-5451
- 11-digit product format
- 007815451
- Labeler code
- 0781
- Product ID
- 0781-5451_5a58b948-d0ce-4f3a-9c10-249c605efcc8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Guanfacine
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Sandoz Inc
- Application
- ANDA202568
- Marketing category
- ANDA
- Marketing start
- 2015-06-03
- Marketing end
- 2019-12-31
- 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