Potassium Chloride Extended-Release - Potassium Chloride 750 mg / 1 Tablet 500 Tablet, Extended Release

Reference details for licensed healthcare facility review and verification.

Potassium Chloride NDC Family 71335-2913 Potassium Chloride 750 mg / 1

NDC 11	71335-2913-01
Product NDC	71335-2913
Generic Drug Name	Potassium Chloride
Brand Name	Potassium Chloride Extended-Release
Manufacturer	Bryant Ranch Prepack
Strength	750 mg / 1
Dosage Form	Tablet
Drug Type	Oral
Package Quantity	500 Tablet, Extended Release
Package Description	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2913-1)
Active Ingredients	Potassium Chloride
Marketing Category	ANDA

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NDC snapshot

Potassium Chloride 750 mg / 1 Tablet is tracked under NDC 71335-2913-01 and rolls up into product family 71335-2913. Use this page to confirm the exact presentation before comparing related family pages or starting a quote review.

Package configuration: 500 Tablet, Extended Release.
Manufacturer: Bryant Ranch Prepack.
Dosage form: Tablet.
Family size: 1 indexed presentation.

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Review the generic familyPotassium Chloride

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Potassium Chloride Extended-Release - Potassium Chloride 750 mg / 1 Tablet 500 Tablet, Extended Release, NDC 71335-2913-01, is a Bryant Ranch Prepack 750 mg / 1 tablet presentation packaged as 500 Tablet, Extended Release.

NDC search formats

Canonical NDC 11: 71335-2913-01
Digits-only NDC 11: 71335291301
Possible 10-digit display format: 71335-2913-1 (7133529131)

Helpful product links

Search by brand name: Potassium Chloride Extended-Release
Exact NDC 11: 71335-2913-01
Product family NDC: 71335-2913
VA classification code: TN430
VA classification code description: POTASSIUM
CMOP ID: P0613
VUID: 4015798