NDC 63187-990 – ciprofloxacin

Ciprofloxacin Hydrochloride 750 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC63187-990

Product details

Brand name
ciprofloxacin
Generic name
ciprofloxacin
Labeler
Proficient Rx LP
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076639
Marketed since
September 10, 2004
Listing expires
December 31, 2026
Pharmacologic class
Quinolone Antimicrobial

Active ingredients

Uses, dosage, side effects and warnings for ciprofloxacin →

Package NDC codes (6)

Package NDCDescriptionSince
63187-990-066 TABLET in 1 BOTTLE (63187-990-06)Mar 1, 2018
63187-990-077 TABLET in 1 BOTTLE (63187-990-07)Mar 1, 2018
63187-990-1010 TABLET in 1 BOTTLE (63187-990-10)Mar 1, 2018
63187-990-1414 TABLET in 1 BOTTLE (63187-990-14)Mar 1, 2018
63187-990-2828 TABLET in 1 BOTTLE (63187-990-28)Mar 1, 2018
63187-990-3030 TABLET in 1 BOTTLE (63187-990-30)Mar 1, 2018

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