Meclizine Hydrochloride
- Product NDC
- 69677-153
- 11-digit product format
- 696770153
- Labeler code
- 69677
- Product ID
- 69677-153_68807858-f249-5aa8-e053-2991aa0a793c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Meclizine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- MAS MANAGEMENT GROUP, INC.
- Application
- ANDA200294
- Marketing category
- ANDA
- Marketing start
- 2012-04-30
- Marketing end
- 0000-00-00
- Substance
- MECLIZINE HYDROCHLORIDE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Antiemetic [EPC],Emesis Suppression [PE]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- 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 |
|---|
| 69677-153-15 | Meclizine Hydrochloride | 15 in 1 BOTTLE | TABLET | 15 | | 1 |
| 69677-153-20 | Meclizine Hydrochloride | 20 in 1 BOTTLE | TABLET | 20 | | 1 |
| 69677-153-30 | Meclizine Hydrochloride | 30 in 1 BOTTLE | TABLET | 30 | | 1 |
| 69677-153-60 | Meclizine Hydrochloride | 60 in 1 BOTTLE | TABLET | 60 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69677-153 | MECLIZINE HYDROCHLORIDE TABLET [MAS MANAGEMENT GROUP, INC.] | 1 | Legacy NDC, 4 package rows | 20180329_68807858-f248-5aa8-e053-2991aa0a793c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 69677-153-15 | 69677015315 | 15 in 1 BOTTLE | Historical |
| 69677-153-20 | 69677015320 | 20 in 1 BOTTLE | Historical |
| 69677-153-30 | 69677015330 | 30 in 1 BOTTLE | Historical |
| 69677-153-60 | 69677015360 | 60 in 1 BOTTLE | Historical |