Guanfacine
- Product NDC
- 68094-019
- 11-digit product format
- 680940019
- Labeler code
- 68094
- Product ID
- 68094-019_056e0dcd-786a-4d81-9b8e-f8b24cb4308a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- guanfacine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Precision Dose, Inc.
- Application
- ANDA075109
- Marketing category
- ANDA
- Marketing start
- 2019-08-05
- Marketing end
- 0000-00-00
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68094-019-62 | 68094001962 | 3 BLISTER PACK in 1 CARTON (68094-019-62) > 10 TABLET in 1 BLISTER PACK (68094-019-59) | 3 blister pack | 2019-08-05 | 0000-00-00 | No | No | Current |