Propafenone Hydrochloride
- Product NDC
- 49884-211
- 11-digit product format
- 498840211
- Labeler code
- 49884
- Product ID
- 49884-211_b87c7717-5019-43fe-9a18-d2d7ae07cc91
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- propafenone hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Par Pharmaceutical, Inc.
- Application
- ANDA078540
- Marketing category
- ANDA
- Marketing start
- 2011-01-03
- Marketing end
- 0000-00-00
- Substance
- PROPAFENONE HYDROCHLORIDE
- Active strength
- 425 mg/1
- Pharmacologic classes
- Antiarrhythmic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 49884-211-01 | 49884021101 | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (49884-211-01) | 2011-01-03 | 0000-00-00 | No | No | Current |
| 49884-211-02 | 49884021102 | 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (49884-211-02) | 2011-01-03 | 2024-09-30 | No | No | Current |
| 49884-211-05 | 49884021105 | 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (49884-211-05) | 2011-01-03 | 2023-08-31 | No | No | Current |
| 49884-211-10 | 49884021110 | 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (49884-211-10) | 2011-01-03 | 0000-00-00 | No | No | Current |