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NDC 69848-0017-02 Guaifenesin 600 mg/1 Details
Guaifenesin 600 mg/1
Guaifenesin is a ORAL TABLET, EXTENDED RELEASE in the HUMAN OTC DRUG category. It is labeled and distributed by GRANULES USA, INC.. The primary component is GUAIFENESIN.
MedlinePlus Drug Summary
Guaifenesin is used to relieve chest congestion. Guaifenesin may help control symptoms but does not treat the cause of symptoms or speed recovery. Guaifenesin is in a class of medications called expectorants. It works by thinning the mucus in the air passages to make it easier to cough up the mucus and clear the airways.
Related Packages: 69848-0017-02Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Guaifenesin
Product Information
| NDC | 69848-0017 |
|---|---|
| Product ID | 69848-017_0ccbb268-ec56-c8eb-e063-6394a90a44b4 |
| Associated GPIs | |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | Guaifenesin |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Guaifenesin |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | TABLET, EXTENDED RELEASE |
| Route | ORAL |
| Active Ingredient Strength | 600 |
| Active Ingredient Units | mg/1 |
| Substance Name | GUAIFENESIN |
| Labeler Name | GRANULES USA, INC. |
| Pharmaceutical Class | Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA213420 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 69848-0017-02 (69848001702)
| NDC Package Code | 69848-017-02 |
|---|---|
| Billing NDC | 69848001702 |
| Package | 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (69848-017-02) |
| Marketing Start Date | 2022-01-06 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |