Curist Mucus Relief
- Product NDC
- 72559-001
- 11-digit product format
- 725590001
- Labeler code
- 72559
- Product ID
- 72559-001_e4a9e3a2-d7bc-31cb-e053-2995a90ab996
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Little Pharma, Inc.
- Application
- ANDA209215
- Marketing category
- ANDA
- Marketing start
- 2019-06-05
- Marketing end
- 0000-00-00
- Substance
- GUAIFENESIN
- Active strength
- 600 mg/1
- Pharmacologic classes
- Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72559-001-03 | 72559000103 | 3 BLISTER PACK in 1 CARTON (72559-001-03) > 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 3 blister pack | 2019-06-05 | 0000-00-00 | No | No | Current |