Smart Sense Mucus Relief ER
- Product NDC
- 49738-325
- 11-digit product format
- 497380325
- Labeler code
- 49738
- Product ID
- 49738-325_8b71fc58-0972-43f5-ae39-c66fbd186924
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Kmart Corporation
- Application
- ANDA091009
- Marketing category
- ANDA
- Marketing start
- 2016-09-01
- Marketing end
- 0000-00-00
- Substance
- GUAIFENESIN
- Active strength
- 1200 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record