verapamil hydrochloride
- Product NDC
- 50436-6916
- 11-digit product format
- 504366916
- Labeler code
- 50436
- Product ID
- 50436-6916_57141d82-27ef-43f2-b41f-7eff9e57219d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- verapamil hydrochloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA090700
- Marketing category
- ANDA
- Marketing start
- 2011-08-05
- Marketing end
- 0000-00-00
- Substance
- VERAPAMIL HYDROCHLORIDE
- Active strength
- 120 mg/1
- Pharmacologic classes
- P-Glycoprotein Inhibitors [MoA],Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC],Cytochrome P450 3A4 Inhibitors [MoA],Cytochrome P450 3A Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 50436-6916-1 | verapamil hydrochloride | 30 in 1 BOTTLE | TABLET, FILM COATED, EXTENDED RE | 30 | | 8 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| VERAPAMIL HYDROCHLORIDE | ACTIVE INGREDIENT | V3888OEY5R | VERAPAMIL HYDROCHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [UNIT DOSE SERVICES] | 4 | |
| VERAPAMIL | ACTIVE MOIETY | CJ0O37KU29 | VERAPAMIL HYDROCHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [UNIT DOSE SERVICES] | 4 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | VERAPAMIL HYDROCHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [UNIT DOSE SERVICES] | 4 | |
| FERRIC OXIDE RED | INACTIVE INGREDIENT | 1K09F3G675 | VERAPAMIL HYDROCHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [UNIT DOSE SERVICES] | 4 | |
| FERRIC OXIDE YELLOW | INACTIVE INGREDIENT | EX438O2MRT | VERAPAMIL HYDROCHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [UNIT DOSE SERVICES] | 4 | |
| FERROSOFERRIC OXIDE | INACTIVE INGREDIENT | XM0M87F357 | VERAPAMIL HYDROCHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [UNIT DOSE SERVICES] | 4 | |
| HYPROMELLOSES | INACTIVE INGREDIENT | 3NXW29V3WO | VERAPAMIL HYDROCHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [UNIT DOSE SERVICES] | 4 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | VERAPAMIL HYDROCHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [UNIT DOSE SERVICES] | 4 | |
| POLYETHYLENE GLYCOL 400 | INACTIVE INGREDIENT | B697894SGQ | VERAPAMIL HYDROCHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [UNIT DOSE SERVICES] | 4 | |
| POVIDONES | INACTIVE INGREDIENT | FZ989GH94E | VERAPAMIL HYDROCHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [UNIT DOSE SERVICES] | 4 | |
| SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | VERAPAMIL HYDROCHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [UNIT DOSE SERVICES] | 4 | |
| SODIUM ALGINATE | INACTIVE INGREDIENT | C269C4G2ZQ | VERAPAMIL HYDROCHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [UNIT DOSE SERVICES] | 4 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | VERAPAMIL HYDROCHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [UNIT DOSE SERVICES] | 4 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50436-6916 | VERAPAMIL HYDROCHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [UNIT DOSE SERVICES] | 8 | Legacy NDC, 1 package rows | 20180612_418751ec-5a65-48cb-b8a8-87172b7183d0.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50436-6916-1 | 50436691601 | 30 in 1 BOTTLE | Historical |