Dalfampridine
- Product NDC
- 51407-246
- 11-digit product format
- 514070246
- Labeler code
- 51407
- Product ID
- 51407-246_44719f12-c2f0-d8ea-e063-6394a90a08cd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dalfampridine
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA206863
- Marketing category
- ANDA
- Marketing start
- 2018-07-11
- Marketing end
- 2026-05-31
- Substance
- DALFAMPRIDINE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Potassium Channel Antagonists [MoA], Potassium Channel Blocker [EPC]
- NDC exclude flag
- No
- Current FDA listing
- Yes
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51407-246-60 | Dalfampridine | 60 in 1 BOTTLE | TABLET, FILM COATED, EXTENDED RE | 60 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51407-246 | DALFAMPRIDINE TABLET, FILM COATED, EXTENDED RELEASE [GOLDEN STATE MEDICAL SUPPLY, INC.] | 6 | Current NDC, Legacy NDC, 1 package rows | 20240302_9b301b27-a182-63d0-e053-2a95a90a10d7.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51407-246-60 | 51407024660 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (51407-246-60) | 2019-12-23 | 2026-05-31 | No | No | Current |