Meclizine Hydrochloride
- Product NDC
- 16571-663
- 11-digit product format
- 165710663
- Labeler code
- 16571
- Product ID
- 16571-663_2be27ea6-3d0a-4036-ab42-fea4720daa34
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Meclizine Hydrochloride
- Dosage form
- TABLET, CHEWABLE
- Route
- ORAL
- Labeler
- Rising Pharma Holdings, Inc.
- Application
- NDA010721
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2020-01-15
- Substance
- MECLIZINE HYDROCHLORIDE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Antiemetic [EPC], Emesis Suppression [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Meclizine Hydrochloride
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MECLIZINE HYDROCHLORIDE | 25 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | HDP7W44CIO |
| Rxcui | 995624, 995632, 995666, 995686 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 16571-663-01 | Meclizine Hydrochloride | 100 in 1 BOTTLE | TABLET, CHEWABLE | 100 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 16571-663 | MECLIZINE HYDROCHLORIDE TABLET MECLIZINE HYDROCHLORIDE TABLET, CHEWABLE [RISING PHARMACEUTICALS, INC.] | 2 | Current NDC, Legacy NDC, 1 package rows | 20221023_c9ddc39c-bc6b-42f1-8c5f-5aff2d79c4bd.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 16571-663-01 | 16571066301 | 100 TABLET, CHEWABLE in 1 BOTTLE (16571-663-01) | 2020-01-15 | 0000-00-00 | No | No | Current |