Guaifenesin
- Product NDC
- 50383-063
- 11-digit product format
- 503830063
- Labeler code
- 50383
- Product ID
- 50383-063_2651ad0c-0f3f-44e2-8273-d480d6f50ecc
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Akorn
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2012-03-07
- Marketing end
- 0000-00-00
- Substance
- GUAIFENESIN
- Active strength
- 100 mg/5mL
- 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
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| GUAIFENESIN | ACTIVE INGREDIENT | 495W7451VQ | GUAIFENESIN SOLUTION [HI-TECH PHARMACAL CO., INC.] | 2 | |
| GUAIFENESIN | ACTIVE MOIETY | 495W7451VQ | GUAIFENESIN SOLUTION [HI-TECH PHARMACAL CO., INC.] | 2 | |
| ACESULFAME POTASSIUM | INACTIVE INGREDIENT | 23OV73Q5G9 | GUAIFENESIN SOLUTION [HI-TECH PHARMACAL CO., INC.] | 2 | |
| ANHYDROUS CITRIC ACID | INACTIVE INGREDIENT | XF417D3PSL | GUAIFENESIN SOLUTION [HI-TECH PHARMACAL CO., INC.] | 2 | |
| ASPARTAME | INACTIVE INGREDIENT | Z0H242BBR1 | GUAIFENESIN SOLUTION [HI-TECH PHARMACAL CO., INC.] | 2 | |
| HYPROMELLOSE 2910 (4000 MPA.S) | INACTIVE INGREDIENT | RN3152OP35 | GUAIFENESIN SOLUTION [HI-TECH PHARMACAL CO., INC.] | 2 | |
| MENTHOL | INACTIVE INGREDIENT | L7T10EIP3A | GUAIFENESIN SOLUTION [HI-TECH PHARMACAL CO., INC.] | 2 | |
| METHYLPARABEN | INACTIVE INGREDIENT | A2I8C7HI9T | GUAIFENESIN SOLUTION [HI-TECH PHARMACAL CO., INC.] | 2 | |
| POTASSIUM SORBATE | INACTIVE INGREDIENT | 1VPU26JZZ4 | GUAIFENESIN SOLUTION [HI-TECH PHARMACAL CO., INC.] | 2 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | GUAIFENESIN SOLUTION [HI-TECH PHARMACAL CO., INC.] | 2 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50383-063 | GUAIFENESIN SOLUTION [AKORN] | 5 | Legacy NDC, 15 package rows | 20221116_5cb704a7-301c-494e-948f-872ee0d5a289.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50383-063-05 | 50383006305 | 5 mL in 1 CUP, UNIT-DOSE | 5 ml | | | | | Historical |
| 50383-063-06 | 50383006306 | 4 TRAY in 1 CASE (50383-063-06) > 10 CUP, UNIT-DOSE in 1 TRAY (50383-063-05) > 5 mL in 1 CUP, UNIT-DOSE | 4 tray | 2012-03-07 | 0000-00-00 | No | No | Current |
| 50383-063-07 | 50383006307 | 10 TRAY in 1 CASE (50383-063-07) > 10 CUP, UNIT-DOSE in 1 TRAY > 5 mL in 1 CUP, UNIT-DOSE | 10 tray | 2012-03-07 | 0000-00-00 | No | No | Current |
| 50383-063-10 | 50383006310 | 10 mL in 1 CUP, UNIT-DOSE | 10 ml | | | | | Historical |
| 50383-063-11 | 50383006311 | 4 TRAY in 1 CASE (50383-063-11) > 10 CUP, UNIT-DOSE in 1 TRAY (50383-063-10) > 10 mL in 1 CUP, UNIT-DOSE | 4 tray | 2012-03-07 | 0000-00-00 | No | No | Current |
| 50383-063-12 | 50383006312 | 10 TRAY in 1 CASE (50383-063-12) > 10 CUP, UNIT-DOSE in 1 TRAY > 10 mL in 1 CUP, UNIT-DOSE | 10 tray | 2012-03-07 | 0000-00-00 | No | No | Current |
| 50383-063-15 | 50383006315 | 10 in 1 TRAY | | | | | | Historical |
| 50383-063-17 | 50383006317 | 4 TRAY in 1 CASE (50383-063-17) > 10 CUP, UNIT-DOSE in 1 TRAY (50383-063-15) > 15 mL in 1 CUP, UNIT-DOSE | 4 tray | 2012-03-07 | 0000-00-00 | No | No | Current |
| 50383-063-18 | 50383006318 | 10 TRAY in 1 CASE (50383-063-18) > 10 CUP, UNIT-DOSE in 1 TRAY > 15 mL in 1 CUP, UNIT-DOSE | 10 tray | 2012-03-07 | 0000-00-00 | No | No | Current |