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NDC 70436-0006-06 Galantamine 12 mg/1 Details
Galantamine 12 mg/1
Galantamine is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Slate Run Pharmaceuticals, LLC. The primary component is GALANTAMINE HYDROBROMIDE.
MedlinePlus Drug Summary
Galantamine is used to treat the symptoms of Alzheimer's disease (AD; a brain disease that slowly destroys the memory and the ability to think, learn, communicate and handle daily activities). Galantamine is in a class of medications called acetylcholinesterase inhibitors. It works by increasing the amount of a certain natural substance in the brain that is needed for memory and thought. Galantamine may improve the ability to think and remember or slow the loss of these abilities in people who have AD. However, galantamine will not cure AD or prevent the loss of mental abilities at some time in the future.
Related Packages: 70436-0006-06Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Galantamine
Product Information
| NDC | 70436-0006 |
|---|---|
| Product ID | 70436-006_085d8e68-8e6f-25d5-e063-6394a90a177a |
| Associated GPIs | 62051030100340 |
| GCN Sequence Number | 046925 |
| GCN Sequence Number Description | galantamine HBr TABLET 12 MG ORAL |
| HIC3 | J1B |
| HIC3 Description | CHOLINESTERASE INHIBITORS |
| GCN | 84853 |
| HICL Sequence Number | 016520 |
| HICL Sequence Number Description | GALANTAMINE HBR |
| Brand/Generic | Generic |
| Proprietary Name | Galantamine |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | galantamine |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET, FILM COATED |
| Route | ORAL |
| Active Ingredient Strength | 12 |
| Active Ingredient Units | mg/1 |
| Substance Name | GALANTAMINE HYDROBROMIDE |
| Labeler Name | Slate Run Pharmaceuticals, LLC |
| Pharmaceutical Class | Cholinesterase Inhibitor [EPC], Cholinesterase Inhibitors [MoA] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA077604 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 70436-0006-06 (70436000606)
| NDC Package Code | 70436-006-06 |
|---|---|
| Billing NDC | 70436000606 |
| Package | 60 TABLET, FILM COATED in 1 BOTTLE (70436-006-06) |
| Marketing Start Date | 2017-08-02 |
| NDC Exclude Flag | N |
| Pricing Information | |
| Price Per Unit | 0.27123 |
| Pricing Unit | EA |
| Effective Date | 2024-02-21 |
| NDC Description | GALANTAMINE HBR 12 MG TABLET |
| Pharmacy Type Indicator | C/I |
| OTC | N |
| Explanation Code | 1 |
| Classification for Rate Setting | G |
| As of Date | 2024-02-21 |