Propafenone Hydrochloride
- Product NDC
- 62559-230
- 11-digit product format
- 625590230
- Labeler code
- 62559
- Product ID
- 62559-230_f3d9c704-c65d-43cd-aafd-2aebe4abfee3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Propafenone Hydrochloride
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- ANI Pharmaceuticals, Inc.
- Application
- ANDA076550
- Marketing category
- ANDA
- Marketing start
- 2015-03-31
- Substance
- PROPAFENONE HYDROCHLORIDE
- Active strength
- 150 mg/1
- Pharmacologic classes
- Antiarrhythmic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Propafenone Hydrochloride
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PROPAFENONE HYDROCHLORIDE | 150 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 33XCH0HOCD |
| Rxcui | 861424, 861427, 861430 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 62559-230-01 | Propafenone Hydrochloride | 100 in 1 BOTTLE | TABLET, COATED | 100 | | 4 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| PROPAFENONE HYDROCHLORIDE | ACTIVE INGREDIENT | 33XCH0HOCD | PROPAFENONE HYDROCHLORIDE TABLET, COATED [ANI PHARMACEUTICALS, INC.] | 1 | |
| PROPAFENONE | ACTIVE MOIETY | 68IQX3T69U | PROPAFENONE HYDROCHLORIDE TABLET, COATED [ANI PHARMACEUTICALS, INC.] | 1 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | PROPAFENONE HYDROCHLORIDE TABLET, COATED [ANI PHARMACEUTICALS, INC.] | 1 | |
| CROSCARMELLOSE SODIUM | INACTIVE INGREDIENT | M28OL1HH48 | PROPAFENONE HYDROCHLORIDE TABLET, COATED [ANI PHARMACEUTICALS, INC.] | 1 | |
| HYPROMELLOSES | INACTIVE INGREDIENT | 3NXW29V3WO | PROPAFENONE HYDROCHLORIDE TABLET, COATED [ANI PHARMACEUTICALS, INC.] | 1 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | PROPAFENONE HYDROCHLORIDE TABLET, COATED [ANI PHARMACEUTICALS, INC.] | 1 | |
| MALTODEXTRIN | INACTIVE INGREDIENT | 7CVR7L4A2D | PROPAFENONE HYDROCHLORIDE TABLET, COATED [ANI PHARMACEUTICALS, INC.] | 1 | |
| POLYDEXTROSE | INACTIVE INGREDIENT | VH2XOU12IE | PROPAFENONE HYDROCHLORIDE TABLET, COATED [ANI PHARMACEUTICALS, INC.] | 1 | |
| POLYETHYLENE GLYCOLS | INACTIVE INGREDIENT | 3WJQ0SDW1A | PROPAFENONE HYDROCHLORIDE TABLET, COATED [ANI PHARMACEUTICALS, INC.] | 1 | |
| POVIDONES | INACTIVE INGREDIENT | FZ989GH94E | PROPAFENONE HYDROCHLORIDE TABLET, COATED [ANI PHARMACEUTICALS, INC.] | 1 | |
| SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | PROPAFENONE HYDROCHLORIDE TABLET, COATED [ANI PHARMACEUTICALS, INC.] | 1 | |
| STARCH, CORN | INACTIVE INGREDIENT | O8232NY3SJ | PROPAFENONE HYDROCHLORIDE TABLET, COATED [ANI PHARMACEUTICALS, INC.] | 1 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | PROPAFENONE HYDROCHLORIDE TABLET, COATED [ANI PHARMACEUTICALS, INC.] | 1 | |
| TRIACETIN | INACTIVE INGREDIENT | XHX3C3X673 | PROPAFENONE HYDROCHLORIDE TABLET, COATED [ANI PHARMACEUTICALS, INC.] | 1 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 62559-230 | PROPAFENONE HYDROCHLORIDE TABLET, COATED [ANI PHARMACEUTICALS, INC.] | 3 | Current NDC, Legacy NDC, 1 package rows | 20181130_8d1be333-be2b-4064-86a4-c2ad9ad07b83.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 |
|---|
| 62559-230-01 | 62559023001 | 100 TABLET, COATED in 1 BOTTLE (62559-230-01) | 2015-03-31 | 0000-00-00 | No | No | Current |