galantamine
- Product NDC
- 68382-179
- 11-digit product format
- 683820179
- Labeler code
- 68382
- Product ID
- 68382-179_ca872164-fc8d-4d1e-aee1-9626e8480cbc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- galantamine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Application
- ANDA078898
- Marketing category
- ANDA
- Marketing start
- 2011-10-10
- Marketing end
- 0000-00-00
- Substance
- GALANTAMINE HYDROBROMIDE
- Active strength
- 12 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 |
|---|
| 68382-179-01 | 68382017901 | 100 TABLET, FILM COATED in 1 BOTTLE (68382-179-01) | | 2011-10-10 | 0000-00-00 | No | No | Current |
| 68382-179-10 | 68382017910 | 1000 TABLET, FILM COATED in 1 BOTTLE (68382-179-10) | | 2011-10-10 | 0000-00-00 | No | No | Current |
| 68382-179-14 | 68382017914 | 60 TABLET, FILM COATED in 1 BOTTLE (68382-179-14) | | 2011-10-10 | 0000-00-00 | No | No | Current |
| 68382-179-77 | 68382017977 | 100 BLISTER PACK in 1 CARTON (68382-179-77) > 1 TABLET, FILM COATED in 1 BLISTER PACK (68382-179-30) | 100 blister pack | 2011-10-10 | 0000-00-00 | No | No | Current |