Guanfacine
- Product NDC
- 72162-1799
- 11-digit product format
- 721621799
- Labeler code
- 72162
- Product ID
- 72162-1799_0fd4fbe8-7bd3-458c-93f2-7fb8f8d3a63d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Guanfacine
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA205689
- Marketing category
- ANDA
- Marketing start
- 2018-08-17
- Substance
- GUANFACINE HYDROCHLORIDE
- Active strength
- 2 mg/1
- Pharmacologic classes
- Adrenergic alpha2-Agonists [MoA], Central alpha-2 Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| PML56A160O | GUANFACINE HYDROCHLORIDE | 29110-48-3 | GUANFACINE HYDROCHLORIDE |
| 30OMY4G3MK | GUANFACINE | 29110-47-2 | Guanfacine |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-1799-1 | 72162179901 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1799-1) | 2018-08-17 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Guanfacine | Bryant Ranch Prepack | 2025-02-04 | HUMAN PRESCRIPTION DRUG LABEL | 102 |