galantamine hydrobromide
- Product NDC
- 10147-0892
- 11-digit product format
- 101470892
- Labeler code
- 10147
- Product ID
- 10147-0892_18d1b4cd-7462-4baa-a561-14bf740d22ee
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- galantamine hydrobromide
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Patriot Pharmaceuticals, LLC
- Application
- NDA021615
- Marketing category
- NDA
- Marketing start
- 2004-12-22
- Marketing end
- 0000-00-00
- Substance
- GALANTAMINE HYDROBROMIDE
- Active strength
- 16 mg/1
- Pharmacologic classes
- Cholinesterase Inhibitor [EPC], Cholinesterase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 10147-0892-3 | 10147089203 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (10147-0892-3) | 2004-12-22 | 0000-00-00 | No | No | Current |