Moexipril Hydrochloride
- Product NDC
- 62135-969
- 11-digit product format
- 621350969
- Labeler code
- 62135
- Product ID
- 62135-969_3001c14d-1545-86fb-e063-6294a90a035f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Moexipril Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Chartwell RX, LLC
- Application
- ANDA077536
- Marketing category
- ANDA
- Marketing start
- 2006-11-30
- Substance
- MOEXIPRIL HYDROCHLORIDE
- Active strength
- 15 mg/1
- Pharmacologic classes
- Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme 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
- Moexipril Hydrochloride
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MOEXIPRIL HYDROCHLORIDE | 15 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | Q1UMG3UH45 |
| Rxcui | 1299896, 1299897 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 62135-969-90 | Moexipril Hydrochloride | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 62135-969 | MOEXIPRIL HYDROCHLORIDE TABLET, FILM COATED [CHARTWELL RX, LLC] | 1 | Current NDC, 1 package rows | 20250312_5c24072c-9769-4cb5-b8da-bf814d21391d.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 62135-969-90 | 62135096990 | 90 TABLET, FILM COATED in 1 BOTTLE (62135-969-90) | 2025-03-05 | No | No | Current |