Galantamine
- Product NDC
- 63739-999
- 11-digit product format
- 637390999
- Labeler code
- 63739
- Product ID
- 63739-999_0cbde513-4342-4737-81f5-17493972aa25
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Galantamine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- McKesson Corporation dba SKY Packaging
- Application
- ANDA090957
- Marketing category
- ANDA
- Marketing start
- 2011-03-29
- Marketing end
- 0000-00-00
- Substance
- GALANTAMINE HYDROBROMIDE
- Active strength
- 4 mg/1
- Pharmacologic classes
- Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63739-999-33 | 63739099933 | 3 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-999-33) > 10 TABLET, FILM COATED in 1 BLISTER PACK | 3 blister pack | 2015-11-04 | 0000-00-00 | No | No | Current |