heartburn relief 150
- Product NDC
- 30142-600
- 11-digit product format
- 301420600
- Labeler code
- 30142
- Product ID
- 30142-600_5c38e419-2260-4d96-8528-d55b2c7c1ded
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Kroger Company
- Application
- ANDA091429
- Marketing category
- ANDA
- Marketing start
- 2013-08-31
- Marketing end
- 2021-07-31
- Substance
- RANITIDINE HYDROCHLORIDE
- Active strength
- 150 mg/1
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 30142-600-01 | 30142060001 | 95 TABLET, FILM COATED in 1 BOTTLE (30142-600-01) | | 2018-04-26 | 0000-00-00 | No | No | Current |
| 30142-600-02 | 30142060002 | 1 BOTTLE in 1 CARTON (30142-600-02) > 24 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2013-11-01 | 0000-00-00 | No | No | Current |
| 30142-600-56 | 30142060056 | 2 BOTTLE in 1 CARTON (30142-600-56) > 95 TABLET, FILM COATED in 1 BOTTLE | 2 bottle | 2018-04-26 | 0000-00-00 | No | No | Current |
| 30142-600-71 | 30142060071 | 1 BOTTLE in 1 CARTON (30142-600-71) > 50 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2013-08-31 | 0000-00-00 | No | No | Current |