VERMOX
- Product NDC
- 50580-070
- 11-digit product format
- 505800070
- Labeler code
- 50580
- Product ID
- 50580-070_3e39b5e3-d0de-4d0d-93a5-071198551c0e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- mebendazole
- Dosage form
- TABLET, CHEWABLE
- Route
- ORAL
- Labeler
- Johnson & Johnson Consumer Inc, McNeil Consumer Healthcare Division
- Application
- NDA017481
- Marketing category
- NDA
- Marketing start
- 1975-01-14
- Marketing end
- 0000-00-00
- Substance
- MEBENDAZOLE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Anthelmintic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 50580-070-12 | 50580007012 | 1 BLISTER PACK in 1 CARTON (50580-070-12) > 12 TABLET, CHEWABLE in 1 BLISTER PACK | 1 blister pack | 1975-01-14 | 0000-00-00 | No | No | Current |