Propafenone Hydrochloride
- Product NDC
- 60687-685
- 11-digit product format
- 606870685
- Labeler code
- 60687
- Product ID
- 60687-685_e64ae05c-783b-d498-e053-2a95a90a9f85
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- propafenone hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA078540
- Marketing category
- ANDA
- Marketing start
- 2022-08-20
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60687-685-32 | 60687068532 | 20 BLISTER PACK in 1 CARTON (60687-685-32) > 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (60687-685-33) | 20 blister pack | 2022-08-20 | 0000-00-00 | No | No | Current |