Albendazole
- Product NDC
- 70710-1021
- 11-digit product format
- 707101021
- Labeler code
- 70710
- Product ID
- 70710-1021_11738578-aa82-4857-8745-9ff4f6b9db13
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Albendazole
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Application
- ANDA208979
- Marketing category
- ANDA
- Marketing start
- 2018-12-17
- Marketing end
- 0000-00-00
- Substance
- ALBENDAZOLE
- Active strength
- 200 mg/1
- Pharmacologic classes
- Anthelmintic [EPC], Cytochrome P450 1A Inducers [MoA]
- 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 |
|---|
| 70710-1021-1 | 70710102101 | 100 TABLET, FILM COATED in 1 BOTTLE (70710-1021-1) | | 2018-12-17 | 0000-00-00 | No | No | Current |
| 70710-1021-3 | 70710102103 | 1 BLISTER PACK in 1 CARTON (70710-1021-3) > 2 TABLET, FILM COATED in 1 BLISTER PACK | 1 blister pack | 2020-05-27 | 0000-00-00 | No | No | Current |
| 70710-1021-5 | 70710102105 | 500 TABLET, FILM COATED in 1 BOTTLE (70710-1021-5) | | 2018-12-17 | 0000-00-00 | No | No | Current |
| 70710-1021-6 | 70710102106 | 2 TABLET, FILM COATED in 1 BOTTLE (70710-1021-6) | | 2020-05-11 | 0000-00-00 | No | No | Current |
| 70710-1021-7 | 70710102107 | 28 TABLET, FILM COATED in 1 BOTTLE (70710-1021-7) | | 2018-12-17 | 0000-00-00 | No | No | Current |
| 70710-1021-8 | 70710102108 | 1 BLISTER PACK in 1 BOTTLE (70710-1021-8) > 2 TABLET, FILM COATED in 1 BLISTER PACK | 1 blister pack | 2018-12-17 | 0000-00-00 | No | No | Current |