Albendazole
- Product NDC
- 16714-907
- 11-digit product format
- 167140907
- Labeler code
- 16714
- Product ID
- 16714-907_64a02ab1-0d8b-4b6c-a1e3-20f5845be97b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Albendazole
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Northstar Rx LLC.
- Application
- ANDA208979
- Marketing category
- ANDA
- Marketing start
- 2019-04-19
- Marketing end
- 2023-02-28
- Substance
- ALBENDAZOLE
- Active strength
- 200 mg/1
- Pharmacologic classes
- Anthelmintic [EPC], Cytochrome P450 1A Inducers [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 16714-907-01 | 16714090701 | 1 BLISTER PACK in 1 BOTTLE (16714-907-01) > 2 TABLET, FILM COATED in 1 BLISTER PACK | 1 blister pack | 2019-04-19 | 2023-02-28 | No | No | Current |
| 16714-907-02 | 16714090702 | 2 TABLET, FILM COATED in 1 BOTTLE (16714-907-02) | | 2020-11-11 | 2023-02-28 | No | No | Current |