mucus er
- Product NDC
- 37808-325
- 11-digit product format
- 378080325
- Labeler code
- 37808
- Product ID
- 37808-325_680203a1-2273-44c5-a219-8bdf373d7c0f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- H E B
- Application
- ANDA091009
- Marketing category
- ANDA
- Marketing start
- 2017-07-12
- Marketing end
- 0000-00-00
- Substance
- GUAIFENESIN
- Active strength
- 1200 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record