AMANTADINE HYDROCHLORIDE
- Product NDC
- 68151-0910
- 11-digit product format
- 681510910
- Labeler code
- 68151
- Product ID
- 68151-0910_01f8a4c6-b19d-49c4-83db-bb6a0f60fef6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- AMANTADINE HYDROCHLORIDE
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Carilion Materials Management
- Application
- ANDA074509
- Marketing category
- ANDA
- Marketing start
- 1995-07-17
- Marketing end
- 0000-00-00
- Substance
- AMANTADINE HYDROCHLORIDE
- Active strength
- 50 mg/5mL
- Pharmacologic classes
- Influenza A M2 Protein Inhibitor [EPC],M2 Protein Inhibitors [MoA]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68151-0910-8 | AMANTADINE HYDROCHLORIDE | 1 mL in 1 BOTTLE | SOLUTION | 1 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68151-0910 | AMANTADINE HYDROCHLORIDE SOLUTION [CARILION MATERIALS MANAGEMENT] | 2 | Legacy NDC, 1 package rows | 20160112_908787d6-159f-486e-a4bb-5d55c14f5c32.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 68151-0910-8 | 68151091008 | 1 mL in 1 BOTTLE | 1 ml | Historical |