Mefloquine Hydrochloride
- Product NDC
- 21695-561
- 11-digit product format
- 216950561
- Labeler code
- 21695
- Product ID
- 21695-561_b6ccbb82-3804-4f02-bf17-f07e22a8b02a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mefloquine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Rebel Distributors Corp
- Application
- ANDA077699
- Marketing category
- ANDA
- Marketing start
- 2010-04-21
- Marketing end
- 0000-00-00
- Substance
- MEFLOQUINE HYDROCHLORIDE
- Active strength
- 250 mg/1
- Pharmacologic classes
- Antimalarial [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 21695-561-10 | Mefloquine Hydrochloride | 10 in 1 BOTTLE | TABLET | 10 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 21695-561 | MEFLOQUINE HYDROCHLORIDE TABLET [REBEL DISTRIBUTORS CORP] | 1 | Legacy NDC, 1 package rows | 20120420_b6ccbb82-3804-4f02-bf17-f07e22a8b02a.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 21695-561-10 | 21695056110 | 10 in 1 BOTTLE | Historical |