51660-054 : Guaifenesin and Dextromethorphan Hydrobromide Oral Tablet, Extended Release

NDC:	51660-054
Labeler:	Ohm Laboratories Inc
Product Type:	Human OTC Drug
Drug Name:	Guaifenesin and Dextromethorphan Hydrobromide
Dosage Form:	Oral Tablet, Extended Release
Application #:	NDA021620
Rev. Date:	Oct 1, 2019

Appearance:

Markings:	xeunciM;1200
Shapes:	Oval
Colors:	White
Size (mm):	22
Segments: ^*	1
^* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines.

NDC Package Codes:

51660-054-41: 1 BLISTER PACK IN 1 CARTON (51660‑054‑41) > 40 TABLET, EXTENDED RELEASE IN 1 BLISTER PACK

Active Ingredients:

Guaifenesin
Dextromethorphan Hydrobromide

Dosage Strength:

600 mg
30 mg

Inactive Ingredients:

Carbomer Homopolymer Type B (Allyl Pentaerythritol Crosslinked)
Hypromellose, Unspecified
Magnesium Stearate
Microcrystalline Cellulose
Sodium Starch Glycolate Type a Potato /

NDC QR Code

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.