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- Product NDC
- 30142-325
- 11-digit product format
- 301420325
- Labeler code
- 30142
- Product ID
- 30142-325_1e2824f0-0c09-4163-8647-31b44e4ff349
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Kroger Company
- Application
- ANDA091009
- Marketing category
- ANDA
- Marketing start
- 2016-03-17
- 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