Citalopram - Hydrobromide 40 mg / 1 Tablet 500 Tablet, Film Coated

Reference details for licensed healthcare facility review and verification.

Citalopram Hydrobromide NDC Family 82009-0108 Citalopram Hydrobromide 40 mg / 1

NDC 11	82009-0108-05
Product NDC	82009-0108
Generic Drug Name	Citalopram Hydrobromide
Brand Name	Citalopram
Manufacturer	Quallent Pharmaceuticals Health Llc
Strength	40 mg / 1
Dosage Form	Tablet
Drug Type	Oral
Package Quantity	500 Tablet, Film Coated
Package Description	500 TABLET, FILM COATED in 1 BOTTLE (82009-108-05)
Active Ingredients	Citalopram Hydrobromide
Marketing Category	ANDA

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NDC snapshot

Citalopram Hydrobromide 40 mg / 1 Tablet is tracked under NDC 82009-0108-05 and rolls up into product family 82009-0108. Use this page to confirm the exact presentation before comparing related family pages or starting a quote review.

Package configuration: 500 Tablet, Film Coated.
Manufacturer: Quallent Pharmaceuticals Health Llc.
Dosage form: Tablet.
Family size: 1 indexed presentation.

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Review the generic familyCitalopram Hydrobromide

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Citalopram - Hydrobromide 40 mg / 1 Tablet 500 Tablet, Film Coated, NDC 82009-0108-05, is a Quallent Pharmaceuticals Health Llc 40 mg / 1 tablet presentation packaged as 500 Tablet, Film Coated.

NDC search formats

Canonical NDC 11: 82009-0108-05
Digits-only NDC 11: 82009010805
Possible 10-digit display formats: 82009-108-05 (8200910805), 82009-0108-5 (8200901085)

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: Citalopram
Exact NDC 11: 82009-0108-05
Product family NDC: 82009-0108
VA classification code: CN609
VA classification code description: ANTIDEPRESSANTS,OTHER
CMOP ID: C0815
VUID: 4013293