NDC 73581-400 – Guaifenesin
Guaifenesin 600 mg/1 · Tablet · Oral
Product NDC73581-400
Product details
- Brand name
- Guaifenesin
- Generic name
- Guaifenesin
- Labeler
- YYBA CORP
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA209215
- Marketed since
- March 10, 2026
- Listing expires
- December 31, 2027
- Pharmacologic class
- Expectorant
Active ingredients
- Guaifenesin 600 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 73581-400-02 | 200 TABLET in 1 BOTTLE (73581-400-02) | Mar 10, 2026 |
| 73581-400-07 | 70 TABLET in 1 BOTTLE (73581-400-07) | Mar 10, 2026 |
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