Pseudoephedrine hydrochloride 120 mg / 1 Tablet 20 Tablet, Extended Release

Reference details for licensed healthcare facility review and verification.

pseudoephedrine hydrochloride NDC Family 51660-0492 pseudoephedrine hydrochloride 120 mg / 1

NDC 11	51660-0492-21
Product NDC	51660-0492
Generic Drug Name	pseudoephedrine hydrochloride
Brand Name	Pseudoephedrine hydrochloride
Manufacturer	Ohm Laboratories Inc.
Strength	120 mg / 1
Dosage Form	Tablet
Drug Type	Oral
Package Quantity	20 Tablet, Extended Release
Package Description	20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (51660-492-21)
Active Ingredients	Pseudoephedrine Hydrochloride
Marketing Category	ANDA

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NDC snapshot

pseudoephedrine hydrochloride 120 mg / 1 Tablet is tracked under NDC 51660-0492-21 and rolls up into product family 51660-0492. 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: 1 indexed presentation.

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Review the generic familypseudoephedrine hydrochloride

Official references

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Pseudoephedrine hydrochloride 120 mg / 1 Tablet 20 Tablet, Extended Release, NDC 51660-0492-21, is a Ohm Laboratories Inc. 120 mg / 1 tablet presentation packaged as 20 Tablet, Extended Release.

NDC search formats

Canonical NDC 11: 51660-0492-21
Digits-only NDC 11: 51660049221
Possible 10-digit display format: 51660-492-21 (5166049221)

Helpful product links

Search by brand name: Pseudoephedrine hydrochloride
Exact NDC 11: 51660-0492-21
Product family NDC: 51660-0492
VA classification code: RE200
VA classification code description: DECONGESTANTS,SYSTEMIC
CMOP ID: P0296
VUID: 4005175