Galantamine Hydrobromide
- Product NDC
- 72162-1447
- 11-digit product format
- 721621447
- Labeler code
- 72162
- Product ID
- 72162-1447_5cd99bc0-0f18-4800-a0f5-a94eebf0eead
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Galantamine Hydrobromide
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA090178
- Marketing category
- ANDA
- Marketing start
- 2011-02-09
- Substance
- GALANTAMINE HYDROBROMIDE
- Active strength
- 16 mg/1
- Pharmacologic classes
- Cholinesterase Inhibitor [EPC], Cholinesterase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| MJ4PTD2VVW | GALANTAMINE HYDROBROMIDE | 1953-04-4 | GALANTAMINE HYDROBROMIDE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-1447-3 | 72162144703 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72162-1447-3) | 2011-02-09 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Galantamine Hydrobromide | Bryant Ranch Prepack | 2024-04-08 | HUMAN PRESCRIPTION DRUG LABEL | 101 |