FOLIC ACID
- Product NDC
- 70518-3198
- 11-digit product format
- 705183198
- Labeler code
- 70518
- Product ID
- 70518-3198_e119519e-c854-4708-e053-2a95a90a2c3e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- FOLIC ACID
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA040796
- Marketing category
- ANDA
- Marketing start
- 2021-08-18
- Marketing end
- 0000-00-00
- Substance
- FOLIC ACID
- Active strength
- 1 mg/1
- 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 |
|---|
| 70518-3198-0 | 70518319800 | 7 TABLET in 1 BLISTER PACK (70518-3198-0) | 7 tablet | 2021-08-18 | 0000-00-00 | No | No | Current |
| 70518-3198-1 | 70518319801 | 30 TABLET in 1 BLISTER PACK (70518-3198-1) | 30 tablet | 2021-09-14 | 0000-00-00 | No | No | Current |
| 70518-3198-2 | 70518319802 | 100 POUCH in 1 BOX (70518-3198-2) > 1 TABLET in 1 POUCH (70518-3198-3) | 100 pouch | 2021-12-08 | 0000-00-00 | No | No | Current |
| 70518-3198-4 | 70518319804 | 30 TABLET in 1 BLISTER PACK (70518-3198-4) | 30 tablet | 2022-06-10 | 0000-00-00 | No | No | Current |