Amantadine Hydrochloride
- Product NDC
- 62135-010
- 11-digit product format
- 621350010
- Labeler code
- 62135
- Product ID
- 62135-010_45c62a1b-f162-d3cb-e063-6394a90a7dbf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amantadine Hydrochloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Chartwell RX, LLC
- Application
- ANDA074028
- Marketing category
- ANDA
- Marketing start
- 1993-06-28
- Substance
- AMANTADINE HYDROCHLORIDE
- Active strength
- 50 mg/5mL
- Pharmacologic classes
- Influenza A M2 Protein Inhibitor [EPC], M2 Protein Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Amantadine Hydrochloride
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| AMANTADINE HYDROCHLORIDE | 50 mg/5mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | M6Q1EO9TD0 |
| Rxcui | 849385 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 62135-010-47 | Amantadine Hydrochloride | 473 mL in 1 BOTTLE | SOLUTION | 473 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 62135-010 | AMANTADINE HYDROCHLORIDE SOLUTION [CHARTWELL RX, LLC] | 4 | Current NDC, Legacy NDC, 1 package rows | 20240524_52aa093c-82cc-4d81-b072-86a2b8adc9c5.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 |
|---|
| 62135-010-47 | 62135001047 | 473 mL in 1 BOTTLE (62135-010-47) | 473 ml | 2022-12-13 | 0000-00-00 | No | No | Current |