Ammonium Lactate
- Product NDC
- 70518-2449
- 11-digit product format
- 705182449
- Labeler code
- 70518
- Product ID
- 70518-2449_e387fee4-16d1-433d-e053-2a95a90a2cc6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ammonium Lactate
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA075774
- Marketing category
- ANDA
- Marketing start
- 2019-11-25
- Marketing end
- 0000-00-00
- Substance
- AMMONIUM LACTATE
- Active strength
- 12 g/100g
- Pharmacologic classes
- Acidifying Activity [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 |
|---|
| 70518-2449-0 | 70518244900 | 2 TUBE in 1 CARTON (70518-2449-0) > 140 g in 1 TUBE | 2 tube | 2019-11-25 | 0000-00-00 | No | No | Current |