Guaifenesin 600 mg / 1 Tablet 20 Tablet, Extended Release

Reference details for licensed healthcare facility review and verification.

Guaifenesin NDC Family 51660-0566 Guaifenesin 600 mg / 1

NDC 11	51660-0566-21
Product NDC	51660-0566
Generic Drug Name	Guaifenesin
Brand Name	Guaifenesin
Manufacturer	Ohm Laboratories, Inc.
Strength	600 mg / 1
Dosage Form	Tablet
Drug Type	Oral
Package Quantity	20 Tablet, Extended Release
Package Description	20 TABLET, EXTENDED RELEASE in 1 CARTON (51660-566-21)
Active Ingredients	Guaifenesin
Marketing Category	ANDA

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NDC snapshot

Guaifenesin 600 mg / 1 Tablet is tracked under NDC 51660-0566-21 and rolls up into product family 51660-0566. Use this page to confirm the exact presentation before comparing related family pages or starting a quote review.

Package configuration: 20 Tablet, Extended Release.
Manufacturer: Ohm Laboratories, Inc..
Dosage form: Tablet.
Family size: 2 indexed presentations.

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Review the generic familyGuaifenesin

Official references

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Alternate presentations in this family

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Guaifenesin 600 mg / 1 Tablet 40 Tablet, Extended ReleaseNDC 51660-0566-41 | 40 Tablet, Extended Release | Ohm Laboratories, Inc.

Potential alternatives with matching presentation

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Guaifenesin 600 mg / 1 Tablet 20 Tablet, Extended Release, NDC 51660-0566-21, is a Ohm Laboratories, Inc. 600 mg / 1 tablet presentation packaged as 20 Tablet, Extended Release.

NDC search formats

Canonical NDC 11: 51660-0566-21
Digits-only NDC 11: 51660056621
Possible 10-digit display format: 51660-566-21 (5166056621)

Helpful product links

Search by brand name: Guaifenesin
Exact NDC 11: 51660-0566-21
Product family NDC: 51660-0566
Other package sizes in this family: 40 Tablet, Extended Release
Compare related presentations: Guaifenesin 600 mg / 1 Tablet 40 Tablet, Extended Release
VA classification code: RE302
VA classification code description: NON-OPIOID-CONTAINING ANTITUSSIVES/EXPECTORANTS
CMOP ID: G0038
VUID: 4007866