NDC 71679-309 – Guaifenesin
Guaifenesin 400 mg/1 · Tablet · Oral
Product NDC71679-309
Product details
- Brand name
- Guaifenesin
- Generic name
- Guaifenesin
- Labeler
- Health Pharma USA LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- OTC MONOGRAPH DRUG · M012
- Marketed since
- February 7, 2024
- Listing expires
- December 31, 2026
- Pharmacologic class
- Expectorant
Active ingredients
- Guaifenesin 400 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 71679-309-00 | 38500 TABLET in 1 BOTTLE (71679-309-00) | Mar 7, 2024 |
| 71679-309-02 | 200 TABLET in 1 BOTTLE (71679-309-02) | Feb 7, 2024 |
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