NDC 68001-561 – Guaifenesin
Guaifenesin 600 mg/1 · Tablet, Extended Release · Oral
Product NDC68001-561
Product details
- Brand name
- Guaifenesin
- Generic name
- Guaifenesin
- Labeler
- BluePoint Laboratories
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA210453
- Marketed since
- March 15, 2023
- Listing expires
- December 31, 2026
- Pharmacologic class
- Expectorant
Active ingredients
- Guaifenesin 600 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 68001-561-17 | 8 BLISTER PACK in 1 CARTON (68001-561-17) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (68001-561-16) | Mar 15, 2023 |
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