Propafenone Hydrochloride
- Product NDC
- 71205-941
- 11-digit product format
- 712050941
- Labeler code
- 71205
- Product ID
- 71205-941_3b289523-f57e-4424-a3ff-d82aeea7a3a2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- propafenone
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA212928
- Marketing category
- ANDA
- Marketing start
- 2020-07-13
- Marketing end
- 0000-00-00
- Substance
- PROPAFENONE HYDROCHLORIDE
- Active strength
- 325 mg/1
- Pharmacologic classes
- Antiarrhythmic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71205-941 | PROPAFENONE HYDROCHLORIDE (PROPAFENONE) CAPSULE, EXTENDED RELEASE [PROFICIENT RX LP] | 2 | Legacy NDC | 20220426_2f2213a9-1164-4ddf-8373-bad78ecbfbfb.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71205-941-60 | 71205094160 | 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71205-941-60) | 2020-11-19 | 0000-00-00 | No | No | Current |