Cimetidine
- Product NDC
- 70934-931
- 11-digit product format
- 709340931
- Labeler code
- 70934
- Product ID
- 70934-931_f174e1bf-fabf-a225-e053-2a95a90abbbf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cimetidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA074151
- Marketing category
- ANDA
- Marketing start
- 2021-11-24
- Marketing end
- 2024-07-31
- Substance
- CIMETIDINE
- Active strength
- 400 mg/1
- Pharmacologic classes
- Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-931-30 | 70934093130 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-931-30) | 2021-11-24 | 0000-00-00 | No | No | Current |