NDC 47335-836 – Galantamine Hydrobromide
Galantamine Hydrobromide 16 mg/1 · Capsule, Extended Release · Oral
Product NDC47335-836
Product details
- Brand name
- Galantamine Hydrobromide
- Generic name
- Galantamine Hydrobromide
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Capsule, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA090178
- Marketed since
- February 9, 2011
- Listing expires
- December 31, 2026
- Pharmacologic class
- Cholinesterase Inhibitor
Active ingredients
- Galantamine Hydrobromide 16 mg/1
Uses, dosage, side effects and warnings for Galantamine Hydrobromide →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 47335-836-08 | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47335-836-08) | Feb 9, 2011 |
| 47335-836-18 | 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47335-836-18) | Feb 9, 2011 |
| 47335-836-83 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47335-836-83) | Feb 9, 2011 |
| 47335-836-88 | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47335-836-88) | Feb 9, 2011 |
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