Guaifenesin
- Product NDC
- 79395-001
- 11-digit product format
- 793950001
- Labeler code
- 79395
- Product ID
- 79395-001_40e84a2d-e25f-4d0d-8b68-d3e01e07a17f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Chalkboard Health
- Application
- ANDA210453
- Marketing category
- ANDA
- Marketing start
- 2020-08-01
- Marketing end
- 0000-00-00
- Substance
- GUAIFENESIN
- Active strength
- 600 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 79395-001-96 | 79395000196 | 1 BLISTER PACK in 1 CARTON (79395-001-96) > 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 1 blister pack | 2020-08-01 | 0000-00-00 | No | No | Current |