Guaifenesin
- Product NDC
- 55319-902
- 11-digit product format
- 553190902
- Labeler code
- 55319
- Product ID
- 55319-902_20b58c6f-969d-4539-a30c-74e5c83a8335
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Family Dollar, Inc.
- Application
- ANDA210453
- Marketing category
- ANDA
- Marketing start
- 2020-09-22
- Marketing end
- 0000-00-00
- Substance
- GUAIFENESIN
- Active strength
- 1200 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 55319-902-64 | 55319090264 | 1 BLISTER PACK in 1 CARTON (55319-902-64) > 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 1 blister pack | 2020-09-22 | 0000-00-00 | No | No | Current |