Albendazole
- Product NDC
- 70771-1103
- 11-digit product format
- 707711103
- Labeler code
- 70771
- Product ID
- 70771-1103_4efbee3c-4848-451c-9744-c3eca20c1c16
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Albendazole
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Zydus Lifesciences Limited
- 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 |
|---|
| 70771-1103-1 | 70771110301 | 100 TABLET, FILM COATED in 1 BOTTLE (70771-1103-1) | | 2018-12-17 | 0000-00-00 | No | No | Current |
| 70771-1103-3 | 70771110303 | 1 BLISTER PACK in 1 CARTON (70771-1103-3) > 2 TABLET, FILM COATED in 1 BLISTER PACK | 1 blister pack | 2020-05-27 | 0000-00-00 | No | No | Current |
| 70771-1103-5 | 70771110305 | 500 TABLET, FILM COATED in 1 BOTTLE (70771-1103-5) | | 2018-12-17 | 0000-00-00 | No | No | Current |
| 70771-1103-6 | 70771110306 | 2 TABLET, FILM COATED in 1 BOTTLE (70771-1103-6) | | 2020-05-11 | 0000-00-00 | No | No | Current |
| 70771-1103-7 | 70771110307 | 28 TABLET, FILM COATED in 1 BOTTLE (70771-1103-7) | | 2018-12-17 | 0000-00-00 | No | No | Current |
| 70771-1103-8 | 70771110308 | 1 BLISTER PACK in 1 BOTTLE (70771-1103-8) > 2 TABLET, FILM COATED in 1 BLISTER PACK | 1 blister pack | 2018-12-17 | 0000-00-00 | No | No | Current |