NDC 72658-0810 – Pregabalin

Pregabalin 75 mg/1 · Capsule · Oral

Human Prescription Drug DEA schedule CV

Product NDC72658-0810

Product details

Brand name
Pregabalin
Generic name
Pregabalin
Labeler
Eskayef Pharmaceuticals Limited
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA212988
Marketed since
April 4, 2022
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Pregabalin →

Package NDC codes (5)

Package NDCDescriptionSince
72658-0810-160 CAPSULE in 1 BOTTLE (72658-0810-1)Apr 4, 2022
72658-0810-290 CAPSULE in 1 BOTTLE (72658-0810-2)Apr 4, 2022
72658-0810-36 BLISTER PACK in 1 CARTON (72658-0810-3) / 10 CAPSULE in 1 BLISTER PACKApr 4, 2022
72658-0810-510 BLISTER PACK in 1 CARTON (72658-0810-5) / 10 CAPSULE in 1 BLISTER PACKApr 4, 2022
72658-0810-6500 CAPSULE in 1 BOTTLE (72658-0810-6)Apr 4, 2022

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