NDC 70771-1075 – Budesonide

Budesonide 3 mg/1 · Capsule, Coated Pellets · Oral

Human Prescription Drug

Product NDC70771-1075

Product details

Brand name
Budesonide
Generic name
Budesonide
Labeler
Zydus Lifesciences Limited
Dosage form
Capsule, Coated Pellets
Route
Oral
Marketing category
ANDA · ANDA206134
Marketed since
June 8, 2017
Listing expires
December 31, 2026
Pharmacologic class
Corticosteroid

Active ingredients

Uses, dosage, side effects and warnings for Budesonide →

Package NDC codes (6)

Package NDCDescriptionSince
70771-1075-01000 CAPSULE, COATED PELLETS in 1 BOTTLE (70771-1075-0)Jun 8, 2017
70771-1075-1100 CAPSULE, COATED PELLETS in 1 BOTTLE (70771-1075-1)Jun 8, 2017
70771-1075-330 CAPSULE, COATED PELLETS in 1 BOTTLE (70771-1075-3)Jun 8, 2017
70771-1075-410 BLISTER PACK in 1 CARTON (70771-1075-4) / 10 CAPSULE, COATED PELLETS in 1 BLISTER PACKJun 8, 2017
70771-1075-5500 CAPSULE, COATED PELLETS in 1 BOTTLE (70771-1075-5)Jun 8, 2017
70771-1075-990 CAPSULE, COATED PELLETS in 1 BOTTLE (70771-1075-9)Jun 8, 2017

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