AMANTADINE HYDROCHLORIDE
- Product NDC
- 24689-112
- 11-digit product format
- 246890112
- Labeler code
- 24689
- Product ID
- 24689-112_d446abf8-c0db-f07f-e053-2995a90a353c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- amantadine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Apnar Pharma LP
- Application
- ANDA210215
- Marketing category
- ANDA
- Marketing start
- 2022-01-20
- Marketing end
- 0000-00-00
- Substance
- AMANTADINE HYDROCHLORIDE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Influenza A M2 Protein Inhibitor [EPC], M2 Protein Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 24689-112-01 | AMANTADINE HYDROCHLORIDE | 100 in 1 BOTTLE | TABLET | 100 | | 2 |
| 24689-112-02 | AMANTADINE HYDROCHLORIDE | 500 in 1 BOTTLE | TABLET | 500 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 24689-112 | AMANTADINE HYDROCHLORIDE TABLET [APNAR PHARMA LP] | 2 | Legacy NDC, 2 package rows | 20240601_d446abf8-c0da-f07f-e053-2995a90a353c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 24689-112-01 | 24689011201 | 100 TABLET in 1 BOTTLE (24689-112-01) | 100 tablet | 2022-01-20 | 0000-00-00 | No | No | Current |
| 24689-112-02 | 24689011202 | 500 TABLET in 1 BOTTLE (24689-112-02) | 500 tablet | 2022-01-20 | 0000-00-00 | No | No | Current |