Tussin
- Product NDC
- 49580-0389
- 11-digit product format
- 495800389
- Labeler code
- 49580
- Product ID
- 49580-0389_f025a3a4-061f-4098-8026-ef6ed47970ab
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- P & L Development, LLC
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2015-02-28
- Marketing end
- 0000-00-00
- Substance
- GUAIFENESIN
- Active strength
- 200 mg/10mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 49580-0389 | TUSSIN ADULT MUCUS AND CHEST CONGESTION (GUAIFENESIN) LIQUID [P & L DEVELOPMENT, LLC] | 5 | Legacy NDC | 20230609_c047f474-3a91-43be-8a20-05af77c1aef8.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 49580-0389-4 | 49580038904 | 1 BOTTLE, PLASTIC in 1 BOX (49580-0389-4) > 118 mL in 1 BOTTLE, PLASTIC | | 2015-02-28 | 0000-00-00 | No | No | Current |
| 49580-0389-5 | 49580038905 | 118 mL in 1 BOTTLE, PLASTIC (49580-0389-5) | 118 ml | 2015-02-28 | 0000-00-00 | No | No | Current |