Galantamine
- Product NDC
- 65841-756
- 11-digit product format
- 658410756
- Labeler code
- 65841
- Product ID
- 65841-756_6ef0e163-f218-4693-b490-a4e863220942
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Galantamine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Zydus Lifesciences Limited
- Application
- ANDA078898
- Marketing category
- ANDA
- Marketing start
- 2011-10-10
- Marketing end
- 0000-00-00
- Substance
- GALANTAMINE HYDROBROMIDE
- Active strength
- 8 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 65841-756-01 | 65841075601 | 100 TABLET, FILM COATED in 1 BOTTLE (65841-756-01) | | 2011-10-10 | 0000-00-00 | No | No | Current |
| 65841-756-10 | 65841075610 | 1000 TABLET, FILM COATED in 1 BOTTLE (65841-756-10) | | 2011-10-10 | 0000-00-00 | No | No | Current |
| 65841-756-14 | 65841075614 | 60 TABLET, FILM COATED in 1 BOTTLE (65841-756-14) | | 2011-10-10 | 0000-00-00 | No | No | Current |
| 65841-756-77 | 65841075677 | 10 BLISTER PACK in 1 CARTON (65841-756-77) > 10 TABLET, FILM COATED in 1 BLISTER PACK | 10 blister pack | 2011-10-10 | 0000-00-00 | No | No | Current |