NDC 71335-9616 – Guaifenesin
Guaifenesin 400 mg/1 · Tablet · Oral
Product NDC71335-9616
Product details
- Brand name
- Guaifenesin
- Generic name
- Guaifenesin
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- OTC MONOGRAPH DRUG · M012
- Marketed since
- August 1, 2020
- Listing expires
- December 31, 2026
- Pharmacologic class
- Expectorant
Active ingredients
- Guaifenesin 400 mg/1
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 71335-9616-1 | 30 TABLET in 1 BOTTLE, PLASTIC (71335-9616-1) | Apr 3, 2024 |
| 71335-9616-2 | 20 TABLET in 1 BOTTLE, PLASTIC (71335-9616-2) | Dec 28, 2022 |
| 71335-9616-3 | 50 TABLET in 1 BOTTLE, PLASTIC (71335-9616-3) | Apr 3, 2024 |
| 71335-9616-4 | 60 TABLET in 1 BOTTLE, PLASTIC (71335-9616-4) | Apr 3, 2024 |
| 71335-9616-5 | 40 TABLET in 1 BOTTLE, PLASTIC (71335-9616-5) | Apr 3, 2024 |
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