Guanfacine
- Product NDC
- 63629-1104
- 11-digit product format
- 636291104
- Labeler code
- 63629
- Product ID
- 63629-1104_c8e508ed-ffa9-45c3-ad34-9428f0574a33
- 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
- Marketing end
- 0000-00-00
- Substance
- GUANFACINE HYDROCHLORIDE
- Active strength
- 3 mg/1
- Pharmacologic classes
- Adrenergic alpha2-Agonists [MoA], Central alpha-2 Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-1104-1 | 63629110401 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-1104-1) | 2022-11-09 | 0000-00-00 | No | No | Current |