Fosaprepitant 150 mg / 1 Injection 1 Injection, Powder, Lyophilized, For Solution

Reference details for licensed healthcare facility review and verification.

fosaprepitant NDC Family 00591-4385 fosaprepitant 150 mg / 1

NDC 11	00591-4385-79
Product NDC	00591-4385
Generic Drug Name	fosaprepitant
Brand Name	Fosaprepitant
Manufacturer	Actavis Pharma, Inc.
Strength	150 mg / 1
Dosage Form	Injection
Drug Type	Intravenous
Package Quantity	1 Injection, Powder, Lyophilized, For Solution
Package Description	1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 CARTON (0591-4385-79)
Active Ingredients	Fosaprepitant Dimeglumine
Marketing Category	NDA

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NDC snapshot

fosaprepitant 150 mg / 1 Injection is tracked under NDC 00591-4385-79 and rolls up into product family 00591-4385. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.

Package configuration: 1 Injection, Powder, Lyophilized, For Solution.
Manufacturer: Actavis Pharma, Inc..
Dosage form: Injection.
Family size: 1 indexed presentation.

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Review the generic familyfosaprepitant

Official references

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Fosaprepitant 150 mg / 1 Injection 1 Injection, Powder, Lyophilized, For Solution, NDC 00591-4385-79, is a Actavis Pharma, Inc. 150 mg / 1 injection presentation packaged as 1 Injection, Powder, Lyophilized, For Solution.

NDC search formats

Canonical NDC 11: 00591-4385-79
Digits-only NDC 11: 00591438579
Possible 10-digit display format: 0591-4385-79 (0591438579)

Helpful product links

Search by brand name: Fosaprepitant
NDC 11: 00591-4385-79
Product family NDC: 00591-4385
VA classification code: GA605
VA classification code description: ANTIEMETICS
CMOP ID: F0477
VUID: 4030308