Buphenyl - Sodium phenylbutyrate 0.94 g / g Powder 1 Bottle

Reference details for licensed healthcare facility review and verification.

sodium phenylbutyrate NDC Family 75987-0070 sodium phenylbutyrate 0.94 g / g

NDC 11	75987-0070-09
Product NDC	75987-0070
Generic Drug Name	sodium phenylbutyrate
Brand Name	Buphenyl
Manufacturer	Horizon Therapeutics USA, Inc.
Strength	0.94 g / g
Dosage Form	Powder
Drug Type	Oral
Package Quantity	1 Bottle
Package Description	1 BOTTLE in 1 CARTON (75987-070-09) / 250 g in 1 BOTTLE
Active Ingredients	Sodium Phenylbutyrate
Marketing Category	NDA

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NDC snapshot

sodium phenylbutyrate 0.94 g / g Powder is tracked under NDC 75987-0070-09 and rolls up into product family 75987-0070. Use this page to confirm the exact presentation before comparing related family pages or starting a quote review.

Package configuration: 1 Bottle.
Manufacturer: Horizon Therapeutics USA, Inc..
Dosage form: Powder.
Family size: 1 indexed presentation.

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Buphenyl - Sodium phenylbutyrate 0.94 g / g Powder 1 Bottle, NDC 75987-0070-09, is a Horizon Therapeutics USA, Inc. 0.94 g / g powder presentation packaged as 1 Bottle.

NDC search formats

Canonical NDC 11: 75987-0070-09
Digits-only NDC 11: 75987007009
Possible 10-digit display formats: 75987-070-09 (7598707009), 75987-0070-9 (7598700709)

Multiple 10-digit display-format aliases can map to the same stored 11-digit billing NDC, so these are shown as search aliases rather than a single asserted package format.

Helpful product links

Search by brand name: Buphenyl
Exact NDC 11: 75987-0070-09
Product family NDC: 75987-0070
VA classification code: AD900
VA classification code description: ANTIDOTES/DETERRENTS,OTHER
CMOP ID: P0447
VUID: 4013035