Acid Reducer
- Product NDC
- 37808-196
- 11-digit product format
- 378080196
- Labeler code
- 37808
- Product ID
- 37808-196_84772d1b-806f-31ec-e053-2a91aa0aeb27
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- HEB
- Application
- ANDA210243
- Marketing category
- ANDA
- Marketing start
- 2018-10-20
- Marketing end
- 0000-00-00
- Substance
- RANITIDINE HYDROCHLORIDE
- Active strength
- 150 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 37808-196-01 | 37808019601 | 1 BOTTLE, PLASTIC in 1 CARTON (37808-196-01) > 24 TABLET in 1 BOTTLE, PLASTIC | 2018-12-31 | 0000-00-00 | No | No | Current |
| 37808-196-04 | 37808019604 | 1 BOTTLE, PLASTIC in 1 CARTON (37808-196-04) > 130 TABLET in 1 BOTTLE, PLASTIC | 2018-12-31 | 0000-00-00 | No | No | Current |