NDC 58602-853 – Guaifenesin
Guaifenesin 600 mg/1 · Tablet, Extended Release · Oral
Product NDC58602-853
Product details
- Brand name
- Guaifenesin
- Generic name
- Guaifenesin
- Labeler
- Aurohealth LLC
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA210453
- Marketed since
- August 13, 2020
- Listing expires
- December 31, 2026
- Pharmacologic class
- Expectorant
Active ingredients
- Guaifenesin 600 mg/1
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 58602-853-12 | 1 BOTTLE in 1 CARTON (58602-853-12) / 40 TABLET, EXTENDED RELEASE in 1 BOTTLE | Aug 13, 2020 |
| 58602-853-21 | 1 BOTTLE in 1 CARTON (58602-853-21) / 100 TABLET, EXTENDED RELEASE in 1 BOTTLE | Aug 13, 2020 |
| 58602-853-73 | 1 BOTTLE in 1 CARTON (58602-853-73) / 20 TABLET, EXTENDED RELEASE in 1 BOTTLE | Aug 13, 2020 |
| 58602-853-96 | 1 BLISTER PACK in 1 CARTON (58602-853-96) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | Aug 13, 2020 |
| 58602-853-97 | 2 BLISTER PACK in 1 CARTON (58602-853-97) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | Aug 13, 2020 |
| 58602-853-98 | 5 BLISTER PACK in 1 CARTON (58602-853-98) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | Nov 1, 2022 |
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