Lactulose
- Product NDC
- 60432-037
- 11-digit product format
- 604320037
- Labeler code
- 60432
- Product ID
- 60432-037_ae4db9a4-d759-436e-ba62-fd2cd158d6c6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lactulose
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Morton Grove Pharmaceuticals, Inc.
- Application
- ANDA074602
- Marketing category
- ANDA
- Marketing start
- 1996-11-14
- Marketing end
- 0000-00-00
- Substance
- LACTULOSE
- Active strength
- 10 g/15mL
- Pharmacologic classes
- Osmotic Laxative [EPC],Osmotic Activity [MoA],Acidifying Activity [MoA],Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60432-037 | LACTULOSE SOLUTION [MORTON GROVE PHARMACEUTICALS, INC.] | 5 | Legacy NDC | 20191105_6c8f865e-f2f4-4c98-8bad-68f1575e2ed5.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60432-037-08 | 60432003708 | 237 mL in 1 BOTTLE, PLASTIC (60432-037-08) | 237 ml | 1996-11-14 | 0000-00-00 | No | No | Current |
| 60432-037-32 | 60432003732 | 946 mL in 1 BOTTLE, PLASTIC (60432-037-32) | 946 ml | 1996-11-14 | 0000-00-00 | No | No | Current |