leader acid control
- Product NDC
- 70000-0375
- 11-digit product format
- 700000375
- Labeler code
- 70000
- Product ID
- 70000-0375_f3f6692d-4e5b-4724-a01f-099acfd203a9
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA076195
- Marketing category
- ANDA
- Marketing start
- 2018-08-27
- Marketing end
- 0000-00-00
- Substance
- RANITIDINE HYDROCHLORIDE
- Active strength
- 75 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 70000-0375-1 | 70000037501 | 1 BOTTLE in 1 CARTON (70000-0375-1) > 65 TABLET, COATED in 1 BOTTLE | 1 bottle | 2018-08-27 | 0000-00-00 | No | No | Current |
| 70000-0375-2 | 70000037502 | 1 BOTTLE in 1 CARTON (70000-0375-2) > 80 TABLET, COATED in 1 BOTTLE | 1 bottle | 2018-08-27 | 0000-00-00 | No | No | Current |