NDC 63187-142 – ciprofloxacin

Ciprofloxacin Hydrochloride 250 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC63187-142

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 (8)

Package NDCDescriptionSince
63187-142-066 TABLET in 1 BOTTLE (63187-142-06)Aug 1, 2014
63187-142-1010 TABLET in 1 BOTTLE (63187-142-10)Aug 1, 2014
63187-142-1414 TABLET in 1 BOTTLE (63187-142-14)Aug 1, 2014
63187-142-2020 TABLET in 1 BOTTLE (63187-142-20)Aug 1, 2014
63187-142-2828 TABLET in 1 BOTTLE (63187-142-28)Aug 1, 2014
63187-142-3030 TABLET in 1 BOTTLE (63187-142-30)Jul 23, 2021
63187-142-6060 TABLET in 1 BOTTLE (63187-142-60)Jul 23, 2021
63187-142-9090 TABLET in 1 BOTTLE (63187-142-90)Jul 23, 2021

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